Corin recalls hip prostheses with incorrect size labels on packaging. The Trinity Biolox Delta Ceramix head is labeled as 36mm instead of 32mm, risking improper fit and complications.
The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa.
Corin is recalling hip prostheses where the size labeled on packaging is incorrect. This could lead to improper fit and potential complications if the wrong size is used during surgery.
The packaging labels incorrectly state the size of the hip prosthesis. The 32mm head is labeled as 36mm and vice versa. This mismatch could lead to improper fit during surgery, potentially causing complications.
Patients who received the recalled hip prosthesis from Corin. Those with the specific model number 104.3615 and lot number :464665 are most at risk.
Check for the model number 104.3615 and lot number 464665 on the packaging. The product is a hip prosthesis with a specific size labeling error.
Look for the model number 104.3615 and lot number 464665 on the packaging to confirm if the product is recalled.
The size indicated on the packaging is incorrect: the Trinity Biolox Delta Ceramix head is labeled as 36mm instead of 32mm.
The model number is 104.3615.
The lot number is 464665.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-1291-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-1291-2021 from Corin. 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.
