Arrow recalls 7Fr catheter clamps with fastener (product code CC-000:13F17B0257) due to unsealed packaging potentially compromising sterility. Affected units may risk infection during medical procedures.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling 7Fr catheter clamps with fastener (product code CC-00007) because the packaging might not be sealed properly. This could lead to contamination and infection if the clamps are used in medical procedures.
The unsealed packaging could allow contaminants to enter the sterile product, increasing the risk of infection during medical procedures. This is a potential sterility issue that could compromise the safety of the device.
Healthcare professionals and patients using the recalled catheter clamps for medical procedures. Those with the specific lot numbers listed are most at risk.
Check for the product code CC-00007 and lot numbers 13F17B0257, 13F17D0260, 13F17E0342, 13F17F0076, 13F17F0795, or 13F17J0271 on the packaging.
Look for the product code CC-00007 and the listed lot numbers on the packaging.
The packaging may not be sealed properly, which could compromise sterility and lead to contamination during medical procedures.
Check the packaging for the product code CC-00007 and lot numbers listed. If you have the affected units, contact Arrow for guidance.
The recall addresses potential contamination risk, not direct injury. Serious injury is not mentioned in the official notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2008-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2008-2018 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.
