DePuy recalls hip implants with a +5mm offset not specified in instructions. This could affect surgical outcomes in hip replacements. Affected models include sizes 41mm-60mm with specific product numbers.
The Cathcart Ball has an inherent +5mm offset which is not currently specified in its Instructions for Use or Surgical Technique Guide. The STG has been updated to reflect the clarification that the +5mm offset should be taken into consideration when using a Cathcart head in a construct for hemi-hip arthroplasty procedures.
DePuy is recalling hip implants that have a +5mm offset not mentioned in their instructions. This could lead to improper surgical placement during hip replacement procedures. The recall affects specific sizes and product numbers.
The hip implant has a +5mm offset that wasn't clearly stated in the surgical instructions. This could cause improper alignment during hip replacement surgery if the offset isn't accounted for, potentially affecting the procedure's outcome.
Orthopedic surgeons and patients who have received the recalled hip implants. The risk is primarily for those undergoing hip replacement surgery with these specific implants.
Check if your hip implant is labeled with sizes 41mm to 60mm. The product numbers listed include 136341000 through 136360000. The recall applies to all units until the instructions are updated.
Review your implant's size and product number to confirm if it matches the recalled range (41mm-60mm) and listed product numbers.
The implant has a +5mm offset not specified in the surgical instructions, which could affect surgical placement during hip replacement procedures.
Check your implant's size and product number to see if it matches the recalled range. No action is needed if the instructions have been updated.
The recall addresses potential surgical misalignment, not direct injury risks to users. The hazard is specific to the surgical procedure.
We’ve drafted a message you can send DePuy to request your refund or repair — edit it as you like.
Subject: Recall Z-1375-2022 — DePuy DePuy Hello, I own a DePuy that is covered by recall Z-1375-2022 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.
