Recall Z-0358-2020— TriMed Inc.

Name: FDA recall Z-0358-2020
Creator: U.S. Food and Drug Administration
Published: 2018-09-28

Class II · Ongoing

Class II FDA medical device recall by TriMed Inc., initiated 2018-09-28. FDA's recall record names no specific 510(k) clearance for this event. Product: TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.. Reason: The spring on the PEG-Extender can rust due to the type of steel used to manufacture it..

Recalling firm: TriMed Inc.
Classification: Class II
Status: Ongoing
Initiated: 2018-09-28
Firm location: Santa Clarita, CA, United States

Product description

TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

Reason for recall

The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.

Data sourced from openFDA. This site is unofficial and independent of the FDA.