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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 96212

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

Open FDA event record

Event summary

Timeline bucket
January 21, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Tyber Medical

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

18 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 18

A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708041

Z-1209-2025
Recall number
Z-1209-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
412 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI; 00196449015528 Lot Numbers 24043BU03, 267844, 24043BU02, 261286

Distribution pattern

Nationwide

device · product 2 of 18

A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate, 4-hole, Right Model/Catalog Number: 770708042

Z-1210-2025
Recall number
Z-1210-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
397

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015535; Lot Numbers 267845, 261287, 265780, 24033BU01

Distribution pattern

Nationwide

device · product 3 of 18

A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate, 6-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708061

Z-1211-2025
Recall number
Z-1211-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
418 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015542; Lot Numbers 267846, 265782, 24043BU04, 261288

Distribution pattern

Nationwide

device · product 4 of 18

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062

Z-1212-2025
Recall number
Z-1212-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
408

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015559; Lot Numbers 265783, 267847, 24036BU02, 261289

Distribution pattern

Nationwide

device · product 5 of 18

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to facilitate healing. Model/Catalog Number: 770708081

Z-1213-2025
Recall number
Z-1213-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
214 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015566; Lot Numbers 265784, 24043BU01, 261290

Distribution pattern

Nationwide

device · product 6 of 18

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate, 8-hole, Right Indicated for use in Fixation of fractures of the distal tibia Model/Catalog Number: 77070802

Z-1214-2025
Recall number
Z-1214-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
212 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015573; Lot Numbers 265785, 24036BU01, 261291

Distribution pattern

Nationwide

device · product 7 of 18

A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770708101

Z-1215-2025
Recall number
Z-1215-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
220 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015580; Lot Numbers 269171, 265809, 262558, 260891

Distribution pattern

Nationwide

device · product 8 of 18

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate, 10-Hole, Right. Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770708102 Product Description:

Z-1216-2025
Recall number
Z-1216-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
219 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015597; Lot Numbers 265810, 260892, 262559

Distribution pattern

Nationwide

device · product 9 of 18

A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708121

Z-1217-2025
Recall number
Z-1217-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015603; Lot Numbers 262560, 260893

Distribution pattern

Nationwide

device · product 10 of 18

A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708122 Product Description:

Z-1218-2025
Recall number
Z-1218-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
115 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015610; Lot Numbers 262571, 260894

Distribution pattern

Nationwide

device · product 11 of 18

A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate, 6-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715061

Z-1219-2025
Recall number
Z-1219-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
197 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015979; Lot Numbers 265790, 263514, 24055DF05, 24056DF01

Distribution pattern

Nationwide

device · product 12 of 18

A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate, 6-Hole, Right Model/Catalog Number: 770715062 Intended for Fixation of fractures of the distal tibia

Z-1220-2025
Recall number
Z-1220-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
210 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015986; Lot Numbers 265792, 24053DF01, 24065DF06, 24052DF01

Distribution pattern

Nationwide

device · product 13 of 18

A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715101

Z-1221-2025
Recall number
Z-1221-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
200 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449015993; Lot numbers 265814, 24060DF02, 24065DF03, 24060DF01. 24065DF05, 263512

Distribution pattern

Nationwide

device · product 14 of 18

A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of fractures of the distal tibia. Model/Catalog Number: 770715102

Z-1222-2025
Recall number
Z-1222-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
209 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449016006; Lot Numbers 265815, 24055DF03, 24055DF04

Distribution pattern

Nationwide

device · product 15 of 18

A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770715121

Z-1223-2025
Recall number
Z-1223-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
201 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449016013; Lot Numbers 265816, 24064DF01, 263557, 24065DF04, 24059DF03, 24059DF02

Distribution pattern

Nationwide

device · product 16 of 18

A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate, 12-Hole, Right Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715122

Z-1224-2025
Recall number
Z-1224-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
208 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449016020; Lot Numbers 265817, 24060DF08, 263511, 24057DF02, 24057DF04

Distribution pattern

Nationwide

device · product 17 of 18

A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate, 16-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715161

Z-1225-2025
Recall number
Z-1225-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
100 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449016037; Lot Numbers 24061DF01, 24065DF02, 24070DF01

Distribution pattern

Nationwide

device · product 18 of 18

A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715162

Z-1226-2025
Recall number
Z-1226-2025
Initiated
January 21, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Tyber Medical
Quantity
109 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices

Code information

UDI-DI 00196449016044; Lot Numbers 24053DF02, 24070DF02, 24057DF01

Distribution pattern

Nationwide

Field note

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