Arrow recalls specific lots of Access Trays and CVC Kits due to potential sterility issues. Affected products may not be completely sealed, risking contamination 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 lots of Access Trays and CVC Kits because they may not be sealed properly, which could lead to contamination during medical procedures. This recall affects healthcare providers using these products in clinical settings.
The recalled products may not be completely sealed, which means the sterility of the catheters cannot be guaranteed. If the seal is compromised, bacteria could enter the catheter during use, potentially causing infections in patients.
Healthcare providers using the recalled Access Trays and CVC Kits in medical procedures are most at risk. Patients receiving procedures with these products could face contamination.
Check for the part numbers: ASK-04001-MS, CDC-12703-1A, CDC-15703-1A, CDC-15703-B1A, CDC-12802-1A, CDC-15802-1A, CDC-17702-1A. Also look for the specific lot numbers listed in the recall notice.
Review the lot numbers listed in the recall notice to determine if your product is affected.
The recalled products may not be completely sealed, which could lead to contamination during medical procedures.
The recall notice does not specify a remedy, so contact Arrow International for further instructions.
The recall is for potential contamination risks during medical procedures, but the notice does not specify patient injuries.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1332-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1332-2018 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.
