Arrow recalls specific Pressure Injectable PICC kits with Chlorag+ard Technology due to potential sterility issues. Affected lots may not be sealed properly, risking infection during medical procedures.
Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
Arrow is recalling certain Pressure Injectable PICC kits that may not be sealed properly, which could lead to contamination during medical procedures. Patients using these kits should contact Arrow for guidance.
The catheters in certain lots may not be completely sealed, which means the sterility of the product cannot be guaranteed. This could lead to contamination during medical procedures if the kit is used.
Patients using the recalled PICC kits for medical procedures are most at risk. Healthcare providers who have these kits in their inventory may also be affected.
Check for part numbers ASK-45541-RWJ4 or ASK-45552-RWJ4. Affected lots include 13F17D0187 and 13F17D0222, 13F17E0849.
Identify the part numbers and lot numbers to confirm if your kit is affected.
Certain lots of cardiovascular catheters may not be completely sealed, so sterility cannot be guaranteed.
The recall does not specify a remedy, so contact Arrow directly for guidance.
Yes, affected lot numbers are 13F17D0187, 13F17D0222, and 13F17E0849.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1327-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1327-2018 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.