DePuy recalls certain CORAIL hip implants due to potential debris behind O-rings. Affected models include specific lot numbers for hip surgery instruments. Contact DePuy for details.
There is the potential for debris/material to be found behind the O-rings in the neck trials.
DePuy is recalling specific hip implants that may have debris behind the O-rings, which could cause complications during surgery. This recall affects certain lot numbers of the CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD) used in hip replacements.
Debris can accumulate behind the O-rings in the neck trials, which are surgical instruments used in hip replacements. This could lead to complications during surgery if the debris interferes with the implant's function.
Surgical patients and medical professionals who use the affected hip implants. The risk is low as the hazard involves potential debris behind O-rings during surgery, not immediate harm.
Check for the product name 'CORAIL AMT STANDARD OFFSET NECK SEGMENT (STD)' with the specific lot numbers listed in the recall notice. These are used in hip replacement surgeries.
Identify the lot numbers from the list provided in the recall notice to determine if your hip implant is affected.
The recall is due to the potential for debris to accumulate behind the O-rings in the neck trials, which could cause complications during hip replacement surgery.
Check the lot numbers listed in the recall notice (e.g., 1212901, 1218481, etc.) to see if your implant matches the affected models.
The recall does not require immediate discontinuation; affected implants should be checked against the listed lot numbers for potential complications.
We’ve drafted a message you can send DePuy to request your refund or repair — edit it as you like.
Subject: Recall Z-1127-2019 — DePuy DePuy Hello, I own a DePuy that is covered by recall Z-1127-2019 from DePuy. 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.
