Arrow recalls specific nerve block needles due to potential sterility compromise from unsealed packaging. Affected units include product codes AB-00090 to AB-17140-N with listed lot numbers.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling certain continuous nerve block needles because the packaging might not be sealed properly, which could lead to contamination. This affects medical devices used for nerve block procedures.
The needles' packaging may not be sealed correctly, potentially allowing contamination. This could lead to infections or other complications if the needles are used without proper sterility.
Healthcare professionals using the needles for medical procedures are most at risk. Patients receiving these needles may be affected if the packaging is compromised.
Check for product codes starting with AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, or AB-18080-N, AB-18110-N. Also look for specific lot numbers listed in the recall notice.
Identify if your needles match the listed product codes: AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, AB-18080-N, AB-18110-N.
Confirm if your needles have any of the listed lot numbers: 13F17G0253, 13F17A0200, 13F17F0505, etc.
The recall is due to potential sterility compromise from unsealed packaging, which could lead to contamination.
Check if your needles match the product codes or lot numbers listed in the recall notice. If they do, contact Arrow for further instructions.
Yes, unsealed packaging could allow contamination, potentially leading to infections or other complications 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-1958-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1958-2018 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.
