Arrow recalls JACC catheters with incorrect expiration dates. Affected units may have safety risks if used beyond the valid date.
Lidstock states the incorrect expiration date for the product
Arrow is recalling JACC catheters that have an incorrect expiration date. Using these catheters after the wrong expiration date could lead to safety issues.
The catheter has an incorrect expiration date, which means it may be unsafe to use after the intended date. This could lead to potential complications if the catheter is used beyond its safe period.
Healthcare professionals and patients using the Arrow JACC catheters with Product Code CDC 42552 JX1A are likely affected. Those who have the catheter and are unsure about the expiration date are at higher risk.
Check for Product Code CDC 42552 JX1A and Batch Code 23F18J0277 on the catheter packaging or label. The recall applies to catheters sold with these specific codes.
Verify the expiration date on the catheter packaging or label to ensure it matches the correct date.
The recall is due to an incorrect expiration date on the catheter, which could lead to safety issues if used beyond the valid date.
Check the expiration date on the catheter packaging or label. If the date is incorrect, contact Arrow for further instructions.
The official recall does not mention a specific fix; the remedy is not stated in the record.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1802-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1802-2019 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.
