Arrow recalls StimuCath Continuous Nerve Block Kit ASK-050:13F18A0547 due to incorrect expiration date on product lidstock. This may lead to improper use of the medical device.
Product lidstock contains the incorrect expiration date for the product
Arrow is recalling a specific nerve block kit because the expiration date on the product lidstock is incorrect. This could lead to improper use of the medical device if the expiration date is not properly noted.
The incorrect expiration date on the product lidstock means the medical device might be used after its expiration date, potentially leading to improper use. This could affect the safety and effectiveness of the nerve block procedure.
Medical professionals who purchased the specific lot number 13F18A0547 of the Arrow StimuCath Continuous Nerve Block Kit ASK-05060-CHO1 are affected. Patients using this kit under medical supervision are at minimal risk.
Check for the lot number 13F18A0547 on the product lidstock of the Arrow StimuCath Continuous Nerve Block Kit ASK-05060-CHO1. The product was sold by Arrow International Inc.
Verify the expiration date on the product lidstock to ensure it matches the correct date for the specific lot number.
The recall is due to an incorrect expiration date on the lidstock, not the product's safety when used correctly.
Check the expiration date on the lidstock; if it's incorrect, contact Arrow International Inc. for guidance.
Look for the lot number 13F18A0547 on the product lidstock of the Arrow StimuCath Continuous Nerve Block Kit ASK-05060-CHO1.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1241-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1241-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.