Arrow recalls Percutaneous Sheath Introducer Kits with unsealed packaging that may compromise sterility. Affected units include specific product codes and lot numbers. Consumers should contact Arrow for details.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Percut: Sheath Introducer Kits that may have unsealed packaging, risking contamination. This could lead to infections if used in medical procedures.
The kits' packaging may not be properly sealed, allowing contaminants to enter. This could compromise sterility during medical procedures, increasing infection risk.
Healthcare professionals using these kits for catheter procedures are most at risk. Patients receiving procedures with these kits could face infection risks.
Check for product code ASK-09907-SB and lot numbers 13F17D0180, 13F17H0192, 13F17K0223, or 13F17K0555. These kits were sold with specific packaging.
Verify the product code and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall is due to potential unsealed packaging that could compromise sterility during medical procedures.
Contact Arrow directly to confirm if your specific kit is affected and follow their instructions.
Yes, unsealed packaging may allow contamination, increasing infection risk during medical procedures.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1977-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1977-2018 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.
