FDAFDA · Food and drugs·Recall number Z-0358-2020
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Published November 20, 2019 · Recall initiated: September 28, 2018
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- TriMed Inc.
- Distributor
- Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden.
- Lot
- Lot number 2858, 2861, and 3749
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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