Ulnar Osteotomy Compression Plate recall
Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and…
Why was Ulnar Osteotomy Compression Plate recalled?
Two instrument holes located on the side of the plate, which act to align the saw guide are located on the wrong side of the plate
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: 10003, 10017
- Product
- Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and…
- Recalling firm
- TriMed Inc.
- Quantity
- 722
- Distribution
- Worldwide Distribution in the state of TX and countries of Australia, China Sweden
- Recall date
- August 29, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)