Exact FDA event identifier

Event 82818

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

Event summary

Timeline bucket: April 18, 2019
Product types: Device
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Zimmer Biomet, Inc.

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

6 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 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420321 Phase 3 Femoral Drill Guide Small

Z-1736-2019

Recall number: Z-1736-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 41 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB160201 ZB160401 ZB161101 ZB170401 ZB170601 ZB170801 ZB170901

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS

device · product 2 of 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420322 Phase 3 Femoral Drill Guide Medium

Z-1737-2019

Recall number: Z-1737-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 10 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB130801

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS

device · product 3 of 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420323 Phase 3 Femoral Drill Guide Large

Z-1738-2019

Recall number: Z-1738-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 11 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB161102 ZB170201 ZB170301 ZB170401 ZB170901

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS

device · product 4 of 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-420324Phase 3 Femoral Drill Guide Extra Large

Z-1739-2019

Recall number: Z-1739-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 3 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB110301

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS

device · product 5 of 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill Guide Extra Small

Z-1740-2019

Recall number: Z-1740-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 14 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB160601 ZB170201 ZB170201 ZB170601

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS

device · product 6 of 6

Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide Small

Z-1741-2019

Recall number: Z-1741-2019
Initiated: April 18, 2019
Classification: Class II
Status: Terminated
Recalling firm: Zimmer Biomet, Inc.
Quantity: 15

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Nonconforming Material/Component

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.

Code information

Lot Numbers: ZB160101 ZB160801 ZB160801

Distribution pattern

CA, IN, LA, NM, NY, TX, WI Foreign: CANADA, AUSTRALIA, JAPAN, NETHERLANDS