TriMed recalls Peg Guide Extenders (REF PEG-XTNDR) due to potential rust from steel spring. Nonsterile, prescription-only device. Check lot numbers 2858, 2861, 3749 for affected units.
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
TriMed is recalling its Peg Guide Extender (REF PEG-XTN: nonsterile, prescription-only) because the steel spring can rust. This could lead to device failure during medical use. Affected units have specific lot numbers.
The spring uses a steel type prone to rusting over time. Rust could weaken the spring, potentially causing the device to malfunction during medical procedures.
People with prescription medical devices using this extender. Those with the specific lot numbers (2858, 2861, 3749) are most at risk.
Check the product label for 'TriMed Peg Guide Extender, REF PEG-XTNDR'. Look for lot numbers 2858, 2861, or 3749 on the packaging.
Look for the lot numbers 2858, 2861, or 3749 on the product packaging.
The recall is due to potential rust from the steel spring, which could cause malfunction. If you have the affected lot numbers, stop using it until you contact TriMed.
Check the lot number on your packaging. If it's 2858, 2861, or 3749, contact TriMed for instructions.
The product is labeled 'TriMed Peg Guide Extender, REF PEG-XTNDR' with lot numbers 2858, 2861, or 3749.
We’ve drafted a message you can send TriMed to request your refund or repair — edit it as you like.
Subject: Recall Z-0358-2020 — TriMed TriMed Hello, I own a TriMed that is covered by recall Z-0358-2020 from TriMed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
