Arrow recalls Maximal Barrier Drape with unsealed packaging that may compromise sterility. Affected product codes include ASK-000:1-1A and specific lot numbers. Consumers should check their items and follow official instructions.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Maximal Barrier Drape products because the packaging may not seal properly, risking contamination. This could lead to sterility issues if the product is used in medical settings. Affected items have specific product codes and lot numbers listed in the recall.
The drape's packaging may not seal correctly, which could allow contaminants to enter the product. This poses a risk to sterility, especially in medical procedures where clean products are critical.
Medical professionals and hospitals using Maximal Barrier Drape products with the listed product codes and lot numbers are most at risk. Consumers who own these items should check their packaging.
Check for product codes starting with ASK-00001-1A and lot numbers: 13F17E0104, 13F17F0318, 13F17G0569, 13F17J0423, or 13F17L0130. The product is sold under the brand Arrow.
Look for product codes starting with ASK-00001-1A and the listed lot numbers on the packaging.
The packaging may not seal properly, which could compromise sterility if used in medical procedures.
Check for product codes starting with ASK-00001-1A and lot numbers: 13F17E0104, 13F17F0318, 13F17G0569, 13F17J0423, or 13F17L0130.
The recall does not specify a remedy, so check with Arrow for further instructions if you have the affected product.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1963-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1963-2018 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.
