Arrow recalls EPIDURAL CATHETERIZATION KIT JH-05500 with incorrect expiration date on product lidstock. Consumers should check for the lot number 13F18A0719 and contact Arrow for details.
Product lidstock contains the incorrect expiration date for the product
Arrow is recalling its EPIDURAL CATHETERIZATION KIT JH-05500 due to an incorrect expiration date on the product lidstock. This could lead to improper use of the medical device if the expiration date is not correctly identified.
The product lidstock contains the incorrect expiration date, which could lead to using the kit after its expiration date has passed. This might affect the sterility and safety of the medical device during procedures.
Healthcare professionals who use the Arrow EPIDURAL CATHETERIZATION KIT JH-05500 are likely affected. Patients receiving epidural procedures using this kit may be at risk if the expiration date is misinterpreted.
Check for the lot number 13F18A0719 on the product lidstock. The kit is sold by Arrow International Inc. and used in epidural procedures.
Look for the lot number 13F18A0719 on the product lidstock to confirm if the kit is affected.
The recall is for the kit itself, not the procedure. If you have the specific lot number, contact Arrow for further instructions.
Check the lot number on the product lidstock; affected kits have lot number 13F18A0719.
Contact Arrow International Inc. directly for guidance on next steps.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1247-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1247-2020 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.