Oxford Femoral Drill Guide Lateral IM Adapter Product recall
Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill guide. The Oxford Fixed Bearing Knee is a Partial knee replacement system…
Why was Oxford Femoral Drill Guide Lateral IM Adapter Product recalled?
Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized diameter that can cause an interference with PN: 32-422822, Oxford Microplasty IM Link.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part Number: 32-423400 Lot Numbers: 238220, 664720,489620, 490930,021410, 507150
- Product
- Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill guide. The Oxford Fixed Bearing Knee is a Partial knee replacement system…
- Recalling firm
- Biomet, Inc.
- Quantity
- 18
- Distribution
- Worldwide Distribution - US Nationwide in the states of NC, IN, PA, OH and the country of the Netherlands.
- Recall date
- July 22, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)