Acumed recalls specific hexalob screw sizes used in wrist fixation systems due to manufacturing errors that may cause screws to break during use. Affected products include 2.7mm and 3.0mm hexalobe screws with reference numbers listed.
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.
Acumed is recalling certain hexalob screws used in wrist fixation systems because manufacturing errors may cause them to break during use. This could lead to complications in medical procedures if the screws fail under stress.
These screws are designed to hold medical implants in place. Manufacturing errors cause them to break under stress during use, which could lead to complications in surgical procedures if the screws fail.
Medical professionals who use these screws for wrist fixation systems are most at risk. Patients undergoing procedures with these screws could face complications if the screws break during surgery.
Check for reference numbers: 3070-27008 to 3076-30014. These screws are used in wrist fixation systems and come in specific sizes like 2.7mm x 8mm to 3.0mm x 14mm.
Look for reference numbers 3070-27008 through 3076-30014 on the screw packaging or documentation.
Reach out to Acumed LLC directly to confirm if your specific screws are affected and get guidance on next steps.
Due to manufacturing errors, these hexalob screws may break during use in wrist fixation systems, potentially causing complications in medical procedures.
The affected screws include sizes from 2.7mm x 8mm to 3.0mm x 14mm, with specific reference numbers listed in the recall notice.
The recall does not require immediate discontinuation; medical professionals should check reference numbers and contact Acumed for guidance.
We’ve drafted a message you can send Acumed to request your refund or repair — edit it as you like.
Subject: Recall Z-2532-2026 — Acumed Acumed Hello, I own a Acumed that is covered by recall Z-2532-2026 from Acumed. 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.
