Edwards Lifesciences recalls Sterile Oxymetry Oligon Catheter Kit (model XA3816SFKT) due to compromised packaging. Affected units have specific lot codes. Consumers should check their kit for packaging issues.
Sterile catheter kit packaging compromised.
Edwards Lifesciences is recalling their Sterile Oxymetry Oligon Catheter Kit because the packaging may be compromised. This could lead to contamination risks if the kit is used without proper sterility. Affected units have specific lot codes listed in the recall.
The catheter kit packaging may be compromised, potentially leading to contamination. If the packaging is not properly sealed, the sterile components could be exposed to contaminants, increasing infection risk during medical procedures.
Healthcare professionals and patients using the Sterile Oxymetry Oligon Catheter Kit for medical purposes. Those with the specific lot codes listed in the recall are most at risk.
Check the lot codes on the packaging: 62563142, 62157774, 62132722, 62749306, or 62625932. The product is a pressure injectable sterile catheter kit with the model number XA3816SFKT.
Inspect the packaging for any signs of damage or compromised seals.
This recall applies to the Sterile Oxymetry Oligon Catheter Kit with specific lot codes. If your kit has one of the listed lot codes, it is affected.
Check the lot codes on your packaging: 62563142, 62157774, 62132722, 62749306, or 62625932. The model number is XA3816SFKT.
Inspect the packaging for damage or compromised seals. If the packaging is compromised, do not use the kit and contact Edwards Lifesciences for further instructions.
We’ve drafted a message you can send Edwards Lifesciences to request your refund or repair — edit it as you like.
Subject: Recall Z-2007-2020 — Edwards Lifesciences Edwards Lifesciences Hello, I own a Edwards Lifesciences that is covered by recall Z-2007-2020 from Edwards Lifesciences. 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.
