Arrow recalls Cannon II Plus Replacement Hub Set with incorrect expiration dates on labels. Using expired products may increase infection risk. Consumers should check product codes and contact Arrow for details.
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 Cannon II Plus Replacement Hub Sets due to incorrect expiration dates on labels. Using these expired products could increase the risk of infection or other complications.
The product labels show an incorrect expiration date. Using expired medical devices can compromise sterility and safety, potentially leading to infections or complications during medical procedures.
Users of Cannon II Plus hub replacement sets who purchased the recalled product codes CAR-02400 with lot numbers 13F19J0153 or 23F17H0547 are affected. Medical professionals using these hubs for surgical connections are most at risk.
Check for product code CAR-02400 and lot numbers 13F19J0153 or 23F17H0547 on the hub set packaging or label. The product is intended for replacing damaged Cannon II Plus hub connections.
Look for product code CAR-02400 and lot numbers 13F19J0153 or 23F17H0547 on the hub set.
The product labels show an incorrect expiration date, which could lead to using expired devices that increase infection risk.
Check for product code CAR-02400 and lot numbers 13F19J0153 or 23F17H0547 on the hub set packaging or label.
The recall does not specify a remedy, so contact Arrow International for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2802-2020 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2802-2020 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.
