Corin recalls specific size 4 dual mobility implants due to packaging issues that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021.
The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.
Corin is recalling certain size 4 dual mobility hip implants because their packaging might get damaged, leading to contamination or loss of sterility. This could affect patients during surgery if the implants aren't properly sterile.
The packaging could become physically damaged or get water exposure, which might cause the implants to lose sterility or become contaminated. This could lead to infections or complications during surgery if the implants aren't properly sterile.
Patients who received these specific hip implants between July 22-26, 2021, from Corin. Surgeons using these implants during procedures in that timeframe are most at risk.
Check for the model numbers 321.04.540 (lot 478880) or 325.04.042 (lot 480567) on the packaging. These implants were shipped between July 22-26, 2021.
Look for model numbers 321.04.540 (lot 478880) or 325.04.042 (lot 480567) on the packaging to confirm if the product is affected.
The packaging could get damaged or exposed to water, which might cause contamination or loss of sterility in the implants.
Check for model numbers 321.04.540 (lot 478880) or 325.04.042 (lot 480567) on the packaging. These implants were shipped between July 22-26, 2021.
The recall record does not specify any action steps for affected products.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-2608-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-2608-2021 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.
