The Oxford recall
The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage…
Why was The Oxford recalled?
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
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?
Biomet Product code: 506076, Lot 829182. Synvasive Part Number: 11-3629.
- Product
- The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage…
- Recalling firm
- Synvasive Technology Inc
- Quantity
- 100 kits
- Distribution
- USA Nationwide Distributor including the state of IN
- Recall date
- April 24, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)