Corin recalls Unity Knee Augments (Size 5-7, 10mm thick) due to packaging risks 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 Unity Knee Augments (sizes 5-7, 10mm thick) because their packaging might cause contamination or loss of sterility. This could lead to infections or complications during surgery if the implants are used without proper sterility.
The packaging system might allow physical damage or water exposure, which could compromise the sterile condition of the implants. If the implants become contaminated, they could cause infections or complications during surgery.
Patients who received these knee implants during surgeries between July 22-26, 2021, are most at risk. The affected units were shipped to hospitals or surgical centers in specific batches.
Check for the product name 'Corin Unity Knee Augments', sizes 5-7, 10mm thick, and the reference number 1122370. Affected units were shipped between July 22-26, 2021.
Inspect the packaging for signs of water damage or physical damage that might compromise sterility.
The recall indicates potential packaging issues that could lead to contamination, but the implants themselves are sterile. Patients should follow the official recall instructions.
The affected units were shipped between July 22-26, 2021.
Check for the product name 'Corin Unity Knee Augments', sizes 5-7, 10mm thick, and reference number 1122370. Affected units were shipped between July 22-26, 2021.
We’ve drafted a message you can send Corin to request your refund or repair — edit it as you like.
Subject: Recall Z-2610-2021 — Corin Corin Hello, I own a Corin that is covered by recall Z-2610-2021 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.
