Arrow International recalls Arrowg+ard Blue Advance JACC product with incorrect expiration date. Consumers should check product code CDC 41552 JX1A for affected units.
Lidstock states the incorrect expiration date for the product
Arrow International is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date. This could lead to product expiration issues, though the recall does not mention specific safety risks.
The product has an incorrect expiration date, which may cause the item to expire prematurely. This could lead to product issues such as reduced effectiveness or potential waste, but the recall does not indicate safety hazards.
Owners of Arrowg+ard Blue Advance JACC products with Product Code CDC 415:52 JX1A and Batch Codes 23F17K0694 or 23F18K0108 are affected. Most at risk are those using the product for extended periods.
Check for Product Code CDC 41552 JX1A and Batch Codes 23F17K0694 or 23F18K0108 on the product label. The product was sold by Arrow International.
Look for Product Code CDC 41552 JX1A and Batch Codes 23F17K0694 or 23F18K0108 on the product label.
The recall is due to an incorrect expiration date on the product, which may cause it to expire prematurely.
Check the product label for Product Code CDC 41552 JX1A and Batch Codes 23F17K0694 or 23F18K0108. If it matches, contact Arrow International for further instructions.
The recall does not mention any safety hazards, only an incorrect expiration date.
We’ve drafted a message you can send Arrow International to request your refund or repair — edit it as you like.
Subject: Recall Z-1798-2019 — Arrow International Arrow International Hello, I own a Arrow International that is covered by recall Z-1798-2019 from Arrow International. 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.