DELTA CER FEM HD 32/0MM T1 Product Usage: For use in recall
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Why was DELTA CER FEM HD 32/0MM T1 Product Usage: For use in recalled?
Product may contain the presence of melted sterile packaging upon opening.
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: 650-1162 lot number: 2016030466
- Product
- DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 30
- Distribution
- US in the state of Texas
- Recall date
- March 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)