Arrow recalls JACC catheters with Chlorag+ard Technology due to incorrect expiration date. Affected units have Product Code CDC 430:23F18A0636. Consumers should contact Arrow for details.
Lidstock states the incorrect expiration date for the product
Arrow is recalling JACC catheters with Chlorag+ard Technology that have an incorrect expiration date. This could lead to product issues if used beyond the valid date.
The catheter has an incorrect expiration date, which could lead to product issues if used beyond the valid date. This might affect the safety and effectiveness of the catheter.
Healthcare professionals using Arrow JACC catheters with Product Code CDC 43063 JX1A and Batch Code 23F18A0636 are most at risk. Patients receiving these catheters may also be affected.
Check for Product Code CDC 43063 JX1A and Batch Code 23F18A0636 on the catheter packaging. The recall applies to Arrow JACC catheters with Chlorag+ard Technology.
Look for Product Code CDC 43063 JX1A and Batch Code 23F18A0636 on the catheter packaging.
The recall is due to an incorrect expiration date for the product, which could lead to product issues if used beyond the valid date.
Check the product code and batch code on the packaging. Contact Arrow for further instructions.
The recall states an incorrect expiration date, but no specific risk of serious injury is mentioned.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1804-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1804-2019 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.
