Arrow International recalls PICCs with Chlorag+ard technology due to incorrect expiration dates on some units. Affected products include specific batch codes and product codes.
Lidstock states the incorrect expiration date for the product
Arrow International is recalling PICCs with Chlorag+ard technology because some units have incorrect expiration dates. This could lead to improper use if the product expires before intended use.
The product has an incorrect expiration date, which could mean the PICC is no longer safe for use after the intended period. This might lead to improper medical treatment if the device expires before the treatment is completed.
Users of the Arrow PICC with Chlorag+:ard technology who purchased the affected batch codes are likely affected. Those using the product for medical purposes may be at slightly higher risk if the expiration date is incorrect.
Check for the product code PR 45552 HPHNM and batch codes 13F17B0178, 13F17C0469, 13F17E0120, 13F17G0412, 13F17H0393, or 13F18A0194 on the device.
Verify the expiration date on the PICC to ensure it matches the intended use period.
The recall is due to incorrect expiration dates on some units, which could lead to improper use if the product expires before intended use.
Batch codes 13F17B0178, 13F17C0469, 13F17E0120, 13F17G0412, 13F17H0393, and 13F18A0194 are affected.
Check for the product code PR 45552 HPHNM and the specific batch codes listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1822-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1822-2019 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.
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.
