Arrow recalls single-shot epidural anesthesia kits with incorrect expiration dates, potentially increasing infection risk. Affected kits may not be sterile or safe beyond the correct expiration date.
The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection or other complications. Sterility, biocompatibility, safety, or efficacy of the kits and their components are not assured beyond the correct expiration date.
Arrow is recalling single-shot epidural anesthesia kits that have an incorrect expiration date on the label. Using these kits could lead to infections or other complications because the products might not be sterile or safe after the expiration date.
The kits have an incorrect expiration date on the label. This means the products could be expired and not sterile or safe for use beyond the correct expiration date, increasing the risk of infection or other complications.
Healthcare professionals who use Arrow Single Shot Epidural Anesthesia Kits with the product code AK-03000-S and lot number 13F17J0230 are affected. Patients receiving epidural anesthesia from these kits may be at risk of infection or complications.
Check for the product code AK-03000-S and lot number 13F17J0230 on the kit. The issue is with the expiration date label on the kit's packaging.
Verify the expiration date on the kit's label to ensure it matches the correct date for the product.
The kit has an incorrect expiration date on the label, which could lead to using an expired product that might not be sterile or safe beyond the correct expiration date.
The product code is AK-03000-S.
The affected lot number is 13F17J0230.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2801-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2801-2020 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.
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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.
