Biomet Arthrosimplicity KIT EU recall
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
Why was Biomet Arthrosimplicity KIT EU recalled?
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
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?
Lot Numbers: 894660A 894660B 894670B 894700B
- Product
- Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
- Recalling firm
- Biomet, Inc.
- Quantity
- 4 units OUS
- Distribution
- Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
- Recall date
- October 14, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)