Arrow recalls Maximal Barrier Drape with unsealed packaging that may compromise sterility. Affected units include specific product codes and lot numbers. Consumers should check their items and contact Arrow for details.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Maximal Barrier Drape products with unsealed packaging that could lead to contamination. This affects medical use items that require sterile conditions, so users should stop using affected units to prevent infection risks.
The drape's packaging may not seal properly, allowing contaminants to enter the sterile product. This could compromise sterility during medical procedures, increasing infection risks for patients and staff.
Healthcare workers and medical facilities using Maximal Barrier Drape for sterile procedures are most at risk. The recall targets specific product codes and lot numbers sold in the U.S.
Check for product codes starting with ASK-00002-1A and lot numbers listed: 13F17A0212, 13F17D0025, 13F17D0154, 13F17E0193, 13F17F0352, 13F17G0102, 13F17G0347, 13F17H0347, 13F17K0324, 13F17K0377, 13F17L0462.
Look for product codes starting with ASK-00002-1A on the drape packaging.
Reach out to Arrow International Inc. for further assistance with affected units.
The drape's packaging may not seal properly, potentially compromising sterility during medical procedures.
Product codes starting with ASK-00002-1A and specific lot numbers: 13F17A0212, 13F17D0025, 13F17D0154, 13F17E0193, 13F17F0352, 13F17G0102, 13F17G0347, 13F17H0347, 13F17K0324, 13F17K0377, 13F17L0462.
The recall is for potential contamination risks, but the remedy does not specify an immediate stop-use action. Check product codes and contact Arrow for guidance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1964-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1964-2018 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.
