Corin recalls specific Trinity Liner ECIMA implants due to packaging issues that may cause water damage, loss of sterility, or contamination. Affected units were 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 two specific Trinity Liner ECIMA implants because their packaging could lead to water damage, loss of sterility, or contamination. This affects patients who received these implants during the specified delivery dates.
The packaging system on these implants could allow water exposure, which might damage the devices, cause loss of sterility, or lead to contamination. This is a risk during handling or storage but not during normal surgical use.
Patients who received the Corin Trinity Liner ECIMA implants between July 22-26, 2021, are most at risk. The affected units were shipped to specific consignees with particular model numbers and lot dates.
Check for model numbers 322.04.640 (lot 479381) or 322.04.936 (lot 479878) on the packaging. These implants were delivered between July 22-26, 2021, to the consignee.
Identify the model number and lot date on the packaging to confirm if the device is affected.
The packaging system on these implants could allow water exposure, potentially causing damage, loss of sterility, or contamination.
Check the model number and lot date on the packaging to see if it's affected. If so, contact Corin for further instructions.
These implants were delivered between July 22-26, 2021, to the consignee.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-2606-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-2606-2021 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.
