Corin recalls specific BIOLOX Delta Mod Head components due to packaging issues that could cause water damage, loss of sterility, or contamination. 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 BIOLOX Delta Mod Head components because their packaging might let water in, which could ruin the sterility or contaminate the devices. This affects implants used in hip surgeries.
The packaging may allow water to enter the sterile component, which could damage the device, cause loss of sterility, or lead to contamination during surgery. This is a risk during the implantation process but not during normal use.
Patients who received the Trinity Acetabular Hip Replacement System with this specific mod head component between July 22-26, 2021. Surgeons and hospitals using these components are most at risk.
Check for the model: Corin BIOLOX Delta Mod Head, diameter 28mm Medium 0mm, 12/14 Taper, REF 104.2805, Sterile. These were shipped to patients between July 22-26, 2021, with lot number 483603 delivered on July 23, 2021.
Look for shipment dates between July 22-26, 2021, and lot number 483603 for the specific mod head component.
The recall addresses packaging risks that could cause water damage, loss of sterility, or contamination during surgery. It does not pose an immediate danger to patients who have already received the implant.
Check for the model: Corin BIOLOX Delta Mod Head, diameter 28mm Medium 0mm, 12/14 Taper, REF 104.2805, Sterile. These were shipped between July 22-26, 2021, with lot number 483603 delivered on July 23, 2021.
The recall does not specify a remedy, so no action is required. However, patients should contact their surgeon if they received this component during the specified shipment dates.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-2607-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-2607-2021 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.
