Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0358-2020 — TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

U.S. FDA — Device Enforcement · United States · 2018-09-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0358-2020
Date of alert
2018-09-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
TriMed Inc.
Product category
device
Product type
Devices
Reported risk: The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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