Arrow recalls Clear Fenestrated Drape with Adhesive (Product Code CD-00001) due to unsealed packaging potentially compromising sterility. Affected lot numbers include 13F17G0258 and 13F17J0281.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling Clear Fenestr:ated Drape with Adhesive because the packaging may not be sealed properly, risking contamination. This could affect medical procedures requiring sterile conditions.
The drape's packaging may not be sealed, which could allow contaminants to enter the sterile environment. This poses a risk of infection during medical procedures that require sterile conditions.
Healthcare professionals using the drape for medical procedures are most at risk. Patients undergoing surgery or other sterile procedures may be affected if the drape is used without proper sterility.
Check for the product code CD-00001 on the packaging. Affected lot numbers are 13F17G0258 and 13F17J0281. The drape has a clear, perforated design with adhesive.
Inspect the packaging for any signs of being unsealed or damaged.
The recall indicates the packaging may not be sealed properly, so it is not recommended for use until the manufacturer confirms it is safe.
The recall does not specify a remedy, so check the packaging for the product code and lot numbers to determine if it is affected.
Affected drape has product code CD-00001 and lot numbers 13F17G0258 or 13F17J0281.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2010-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2010-2018 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.
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.
