Arrow recalls specific lots of Endurance Extended Dwell Peripheral Catheters due to potential sterility issues. Affected units may not be sterile, risking infection during medical procedures.
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
Arrow is recalling specific lots of Endurance Extended Dwell Peripheral Catheters because they may not be sterile, which could lead to infections during medical procedures. Patients using these catheters should contact Arrow for details.
The catheters in specific manufacturing lots may not be sterile, which could lead to infections if used during medical procedures. This is a potential sterility issue that could compromise patient safety.
Patients using the recalled catheters for medical procedures are affected. Healthcare providers who use these specific lots for treatments are at risk of potential infection.
Check for the product code ASK-00820-FLH and manufacturing lots 13F19E0247, 13F19F0006, or 13F19G0433. The catheters were sold with expiration dates from August to September 2020.
Identify the product code ASK-00820-FLH and manufacturing lots 13F19E0247, 13F19F0006, or 13F19G0433 to confirm if your catheter is affected.
The recall is due to a potential sterility issue in specific manufacturing lots, which could lead to infections during medical procedures.
Contact Arrow directly to check if your catheter is affected and follow their instructions.
The catheters may not be sterile, which could lead to infections during medical procedures, but the recall is for specific lots only.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0837-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0837-2020 from Arrow. 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.
