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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82377

26 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 08, 2019
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Integra LifeSciences Corp.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

26 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 26

Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T

Z-1150-2019
Recall number
Z-1150-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180072 181145 184085 184086

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 2 of 26

Salto Talaris Tibial Ankle Prosthesis Tray, Talar Dome, Size 1, Right, Part No. LJU201T

Z-1151-2019
Recall number
Z-1151-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

181146 181718

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 3 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T

Z-1152-2019
Recall number
Z-1152-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180073 181259 182899

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 4 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Right, Part No. LJU203T

Z-1153-2019
Recall number
Z-1153-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

181155 182900

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 5 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Left, Part No. LJU210T

Z-1154-2019
Recall number
Z-1154-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180074 181260 182901 184538

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 6 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 1, Left, Part No. LJU211T

Z-1155-2019
Recall number
Z-1155-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180859

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 7 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Left, Part No. LJU212T

Z-1156-2019
Recall number
Z-1156-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

181147 181719 181720 183669

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 8 of 26

Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 3, Left, Part No. LJU213T

Z-1157-2019
Recall number
Z-1157-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180075 181348

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 9 of 26

Tibial Total Ankle Prosthesis Tray, Size 0, Product No. LJU220T

Z-1158-2019
Recall number
Z-1158-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

181148

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 10 of 26

Tibial Total Ankle Prosthesis Tray, Size 1, Product No. LJU221T

Z-1159-2019
Recall number
Z-1159-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180750 180860 180861 180892 181432

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 11 of 26

Tibial Total Ankle Prosthesis Tray, Size 2, Product No. LJU222T

Z-1160-2019
Recall number
Z-1160-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180751 180893 181149 181150 181151 185084 180894

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 12 of 26

Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T

Z-1161-2019
Recall number
Z-1161-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180894 181152

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 13 of 26

Talar Dome Total Ankle Prosthesis, Flat Cut, Size 1, Left, Product No. LJU821T

Z-1162-2019
Recall number
Z-1162-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180079 181349

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 14 of 26

Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Left, Product No. LJU822T

Z-1163-2019
Recall number
Z-1163-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180080 182904 183671 184878

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 15 of 26

Talar Dome Total Ankle Prosthesis , Flat Cut, Size 3, Left, Product No. LJU823T

Z-1164-2019
Recall number
Z-1164-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180081

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 16 of 26

Talar Dome Total Ankle Prosthesis , Flat Cut, Size 1, Right, Product No. LJU811T

Z-1165-2019
Recall number
Z-1165-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180076 180082 185085

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 17 of 26

Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Right, Product No. LJU812T

Z-1166-2019
Recall number
Z-1166-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180077 182902 185086

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 18 of 26

Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T

Z-1167-2019
Recall number
Z-1167-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

180078 182903 183670 190799

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 19 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T

Z-1168-2019
Recall number
Z-1168-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182853 182854 183344

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 20 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T

Z-1169-2019
Recall number
Z-1169-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182855 182856 183397

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 21 of 26

Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T

Z-1170-2019
Recall number
Z-1170-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182857 182858 183345 183346

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 22 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T

Z-1171-2019
Recall number
Z-1171-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182859 183347 183348

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 23 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Left, Product No. LJV190T

Z-1172-2019
Recall number
Z-1172-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

183349

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 24 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T

Z-1173-2019
Recall number
Z-1173-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182860 182861 183350 183351

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 25 of 26

Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T

Z-1174-2019
Recall number
Z-1174-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182862 183352 183353

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

device · product 26 of 26

Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Left, Product No. LJV193T

Z-1175-2019
Recall number
Z-1175-2019
Initiated
March 08, 2019
Classification
Class II
Status
Terminated
Quantity
2029

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

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Inspect official wording and provenance

Reason for recall

The Salto Talaris and Integra XT Revision implant labelling was found to list an incorrect metallic coating material symbol on the metallic implant labels (box and inner pouch) and IFU

Code information

182863 182864 183354

Distribution pattern

Distributors in AL, CA, CT, FL, GA, HI, IA, ID, KS, KY, MD, MI, MO, MT, NC, NE, NJ, NM, NY, OH, OK,PA, TX, VA, WA, and WI.

Field note

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