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TriMed Inc. recalls TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Recalled November 20, 2019 · FDA recall Z-0358-2020 · TriMed
Hazard
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it. · FDA Class II
Units
1,903 Peg Guide Extenders
Sold at
Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden.
Description
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Product
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Manufacturer(s)
TriMed Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →