TriMed recalls 3.6mm threaded IM nails with a driver-socket that may not apply sufficient torque, risking improper use. Affected items have specific model numbers and lot codes.
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
TriMed is recalling threaded IM nails that may not apply enough torque due to a faulty driver-socket. This could lead to improper use, but the risk is not immediately dangerous.
The driver-socket in the nail system is out of specification, which might prevent proper application of torque. This could lead to nails not being securely fastened during use.
Medical professionals who use these nails for injections are most at risk. Patients using these products are not affected since they require a prescription.
Check for model numbers IMN3.6-60 T or IMN3.6-65 T with lot number QM23086. These nails are sold with a prescription and non-sterile packaging.
Look for model numbers IMN3.6-60 T or IMN3.6-65 T and lot number QM23086 on the packaging.
The driver-socket is out of specification and may not apply sufficient torque, potentially causing improper use.
Check for model numbers IMN3.6-60 T or IMN3.6-65 T with lot number QM23086 on the packaging.
No specific action is required; the recall is for identification and potential correction if needed.
We’ve drafted a message you can send TriMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1791-2024 — TriMed TriMed Hello, I own a TriMed that is covered by recall Z-1791-2024 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.
