SEASPINE ORTHOPEDICS CORPORATION recalls Meridian Angled Awl Fixed (model RA2-003015) due to insufficient weld around cap component, which may fail under impact forces.
Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
SEASPINE ORTHOPEDICS CORPORATION is recalling Meridian Angled Awl Fixed surgical instruments with model number RA2-003015 because the weld around the cap component is too weak to handle impact forces. This could lead to the instrument failing during use, potentially causing injury.
The weld around the cap component is too weak to withstand impact forces. If the instrument is struck or subjected to force during use, the weld could fail, causing the instrument to break or detach.
Surgical professionals and medical facilities that own or use the Meridian Angled Awl Fixed (model RA2-003015) are affected. Those using the instrument in procedures where it might experience impact forces are at higher risk.
Check for the model number RA2-003015 on the Meridian Angled Awl Fixed product. The lot numbers TT0190H and TT0191H are also associated with this recall.
Verify the model number RA2-003015 and lot numbers TT0190H or TT0191H on the instrument.
The recall states the weld around the cap component may fail under impact forces, which could lead to injury. However, the remedy is not specified, so users should check if they have the recalled model.
The recall does not provide a specific remedy. Check the model number and lot numbers to confirm if your product is affected.
Look for the model number RA2-003015 and lot numbers TT0190H or TT0191H on the Meridian Angled Awl Fixed product.
We’ve drafted a message you can send Meridian to request your refund or repair — edit it as you like.
Subject: Recall Z-2357-2024 — Meridian Meridian Hello, I own a Meridian that is covered by recall Z-2357-2024 from Meridian. 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.
