Arrow recalls Peel Away Sheath over Dilator (product codes PL-05041, PL-05052) due to unsealed packaging potentially compromising sterility. Affected units include specific lot numbers listed in the recall notice.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Peel Away Sheath over Dilator products with specific codes because the packaging might not be sealed properly. This could lead to contamination, which is a serious risk for medical procedures.
The packaging may not be sealed correctly, which could allow contamination of the product. This is a risk during medical procedures where sterility is critical.
Medical professionals and patients using the Peel Away Sheath over Dilator for procedures are affected. Those with the specific product codes and lot numbers listed in the recall are most at risk.
Check for product codes PL-05041 or PL-05052 on the packaging. Lot numbers include specific sequences like 13F17G0050 for PL-05041 and 13F17C0435 for PL-05052.
Look for product codes PL-05041 or PL-05052 on the packaging.
The packaging may not be sealed properly, which could lead to contamination during medical procedures.
The recall notice does not specify a remedy, so contact Arrow International for guidance.
Check for product codes PL-05041 or PL-05052 and specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2021-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2021-2018 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.
