Arrow recalls Echogenic Introducer Needles (AN-04318) with unsealed packaging that may compromise sterility. Affected lot numbers include 13F17A0231 through 13F17L0233. Consumers should check their product labels for these specific lot numbers.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Echogenic Introducer Needles with unsealed packaging that could compromise sterility. This risk means the needles might not be sterile when used, potentially causing infections during medical procedures.
The needles' packaging may not be properly sealed, which could allow contamination. If the packaging is not sterile, using the needles could lead to infections during medical procedures.
Medical professionals and patients using the Echogenic Introducer Needles with unsealed packaging. Those who have the specific lot numbers listed in the recall are most at risk.
Check the product label for the lot numbers listed: 13F17A0231 through 13F17L0233. The product code is AN-04318. These needles were sold by Arrow International Inc.
Look for the lot numbers 13F17A0231 through 13F17L0233 on the product label to confirm if your needle is affected.
The needles' packaging may not be properly sealed, which could allow contamination and compromise sterility.
Check your product label for the lot numbers listed. If you have these specific lot numbers, you should stop using the needles and contact Arrow for further instructions.
The recall does not specify a fix; the remedy is null, so consumers should check their product labels and contact Arrow if needed.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1959-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1959-2018 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.
