CER Bioloxd Option HD 32mm recall
CER BIOLOXD OPTION HD 32MM, model # 650-1056
Why was CER Bioloxd Option HD 32mm recalled?
Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.
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 Number: 843260
- Product
- CER BIOLOXD OPTION HD 32MM, model # 650-1056
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- N/A
- Distribution
- Nationwide in US; Internationally Argentina, Netherlands & Canada
- Recall date
- January 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)