Smith & Nephew recalls 5.5mm FOOTPRINT Ultra PK Suture Anchors with specific part numbers due to potential displacement of the anchor tip protector, risking sterile breaches during medical procedures.
Space between the device and the packaging permits excessive movement which could potentially lead to the displacement of the anchor s tip protector allowing the tip of the anchor to create a sterile breach.
Smith & Nephew is recalling certain 5.5mm FOOTPRINT Ultra PK Suture Anchors because a gap between the device and packaging could cause the anchor tip protector to displace, potentially creating a sterile breach during surgery. This risk affects medical professionals using the product in surgical settings.
The device has a space between it and the packaging that allows excessive movement. This movement could displace the anchor tip protector, causing the anchor tip to create a sterile breach during surgery.
Medical professionals who use the recalled suture anchors during surgical procedures are most at risk. Patients undergoing surgery with these anchors could face potential sterile breaches.
Check for the product name 'FOOTPRINT Ultra PK Suture Anchor', 5.5mm size, and part number 72202902. The recall includes specific lot numbers listed in the record.
Identify the product name, size, and part number to confirm if it's recalled.
The recalled product has part number 72202902.
Check for the product name 'FOOTPRINT Ultra PK Suture Anchor', 5.5mm size, and part number 72202902. The recall includes specific lot numbers listed in the record.
The recall record does not specify a remedy.
We’ve drafted a message you can send Smith & Nephew to request your refund or repair — edit it as you like.
Subject: Recall Z-1757-2020 — Smith & Nephew Smith & Nephew Hello, I own a Smith & Nephew that is covered by recall Z-1757-2020 from Smith & Nephew. 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.
