Arrow International recalls JACC central catheters with Chlorag+ard technology due to incorrect expiration dates. Affected units have Product Code CDC 42563 JX1A and Batch Codes 23F17E0686 or 2:3F18H0290.
Lidstock states the incorrect expiration date for the product
Arrow International is recalling JACC central catheters with Chlorag+ard technology because they have an incorrect expiration date. This could lead to product expiration issues, but the recall does not mention specific safety risks or injuries.
The product has an incorrect expiration date, which could lead to the catheter expiring before use. This might cause issues with the product's effectiveness or safety, but the recall does not specify any immediate health risks.
Healthcare professionals who use Arrow JACC central catheters with Product Code CDC 42563 JX1A and Batch Codes 23F17E0686 or 23F18H0290 are likely affected. Patients receiving these catheters may also be impacted.
Check for Product Code CDC 42563 JX1A and Batch Codes 23F17E0686 or 23F18H0290 on the catheter packaging. The recall applies to these specific models sold by Arrow International.
Verify the Product Code CDC 42563 JX1A and Batch Codes 23F17E0686 or 23F18H0290 on the catheter packaging.
The recall is due to an incorrect expiration date on the product, which could lead to expiration issues.
Check the Product Code and Batch Codes on the packaging to see if it is affected. If it is, contact Arrow International for further instructions.
The recall does not mention any specific safety risks or injuries, only an incorrect expiration date.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1803-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1803-2019 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.
