Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for ...
FDA Device Recall #Z-1161-2017 — Class II — January 5, 2016
Recall Summary
| Recall Number | Z-1161-2017 |
| Classification | Class II — Moderate risk |
| Date Initiated | January 5, 2016 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Biomet U.K., Ltd. |
| Location | Bridgend South Wales, N/A |
| Product Type | Devices |
| Quantity | 72 units in total |
Product Description
Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Reason for Recall
Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.
Distribution Pattern
Worldwide Distribution in the states of LA, NC, AR, MT, MO, CA, NY, KS, TX, MA, KY, OK, SC, NJ and the countries of Foreign: THAILAND, JAPAN, NETHERLANDS
Lot / Code Information
Item: 32-420736, Lots: ZB160501, ZB160601
Other Recalls from Biomet U.K., Ltd.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-1169-2017 | Class II | Oxford Unicompartmental Knee Phase 3 Shim Size ... | Jan 5, 2016 |
| Z-1164-2017 | Class II | Oxford Partial Knee System Right Medial Tibial ... | Jan 5, 2016 |
| Z-1156-2017 | Class II | Oxford Partial Knee System Right Medial Tibial ... | Jan 5, 2016 |
| Z-1175-2017 | Class II | Oxford Partial Knee System Phase 3 Tibial Templ... | Jan 5, 2016 |
| Z-1160-2017 | Class II | Oxford Partial Knee System Right Medial Tibial ... | Jan 5, 2016 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.