TriMed Wrist Hook Dorsal Impactor recall
TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the…
Why was TriMed Wrist Hook Dorsal Impactor recalled?
The WHD/WHV impactors can rust over time due to an improper manufacturing process.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 049045, 049044, and 049044R1.
- Product
- TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the…
- Recalling firm
- TriMed Inc.
- Quantity
- 561 devices
- Distribution
- Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden.
- Recall date
- November 20, 2019
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)