Corin recalls specific TriFit TS surgical implants due to packaging issues that could cause contamination or loss of sterility. Affected units shipped between July 22-26, 2021, with lot number 467870.
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 TriFit TS surgical implants because their packaging might cause contamination or loss of sterility. This could lead to infections or complications during surgery if the device is used without proper sterility.
The packaging system could allow physical damage or water exposure, which might compromise the device's sterility. This could lead to contamination during surgical procedures if the device is not properly sterilized.
Surgical patients and medical professionals who received the specific TriFit TS Size 8 implants with lot number 467870 or shipped between July 22-26, 2021. Patients using these implants during surgery are at risk of infection.
Check for the product name 'Corin TriFit TS', size 8, standard tapered stem, and reference number 694.0008. The affected units were shipped between July 22-26, 2021, with lot number 467870.
Identify if your device matches the product name, size, reference number, and shipment dates described in the recall.
The recall addresses potential contamination or loss of sterility due to packaging issues, but the risk is low if proper handling is followed.
Check for the product name 'Corin TriFit TS', size 8, reference number 694.0008, and shipment dates between July 22-26, 2021, with lot number 467870.
The recall does not require immediate discontinuation; however, you should check if your device is affected before use.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-2603-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-2603-2021 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.
