TriMed Peg Guide Extender — Class II medical device recall Z-0358-2020
Ongoing recall by TriMed Inc., reported 2019-11-20, distributed nationwide. The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
| Recall number | Z-0358-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TriMed Inc., Santa Clarita, CA, United States |
| Recall initiated | 2018-09-28 |
| Classified | 2019-11-12 |
| Reported by FDA | 2019-11-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CN, SE, ZA |
| Quantity | 1,903 peg |
| Lot numbers | 2858, 2861, 3749 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0358-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.