Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product where injury has not yet been reported, fitting the criteria for a High severity score.
Plain-English summary
Biomet U.K., Ltd. is conducting a medical device field action for various lot-specific Oxford Knee instruments. The affected products are Oxford Partial Knee System Left Medial Tibial Trial Tray Size F instruments, used with the Oxford Uni Partial Knee System. The recall involves 72 units in total, specifically item 32-420822 from lots ZB160501, ZB160601, and ZB160701.
The recall is being conducted due to potential alumina inclusions in the raw material batch used to produce the affected products. These inclusions contained within the finished product could lead to the cracking and separation of the instrument.
The affected products were distributed worldwide, including in the United States states of LA, NC, AR, MT, MO, CA, NY, KS, TX, MA, KY, OK, SC, and NJ, as well as in Thailand, Japan, and the Netherlands. Healthcare providers and facilities should stop using the affected instruments and contact Biomet U.K., Ltd. for further instructions.
The recalled product
- Product
- Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
- Manufacturer
- Biomet U.K., Ltd.
- Affected units
- 72
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Item: 32-420822
- Lots: ZB160501 ZB160601 ZB160701
Distribution
Part of a larger recall action
This product is one of 24 recalled by Biomet U.K., Ltd. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 24 products in this recall →Related recalls
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