TriMed Peg Guide Extender recall
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Why was TriMed Peg Guide Extender recalled?
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
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 number 2858, 2861, and 3749
- Product
- TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
- Recalling firm
- TriMed Inc.
- Quantity
- 1,903 Peg Guide Extenders
- 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)