ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp recall
ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical…
Why was ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp recalled?
Potential issue associated with the instrument -end of the shaft could fail to effectively mate with the broach
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: 827310, 711160, 203240
- Product
- ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orthopedic manual surgical…
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 67 units
- Distribution
- US Nationwide and Foreign: countries of Canada, CHINA, NETHERLANDS
- Recall date
- February 5, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)