Arrow recalls disposable pain control pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief and needing extra medication.
Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This may result in the need for other, additional analgesic drug administration.
Arrow is recalling disposable pain control pumps that may have cracks in the fill port connector. This could cause leaks during use, potentially reducing pain relief and requiring additional medication.
The fill port connector may crack, causing leaks. If the leak happens while filling the pump, it could delay finding a replacement. If undetected, it might reduce drug delivery, leading to less pain relief than prescribed and possibly needing extra medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management are most at risk if the pump has a leak. The recall affects specific model numbers sold with certain product codes.
Check for the product code MC0050XLSK5 CP on the pump. The pump model is AF 550 x 5ML/H 6" CATH, 4.5" IN. This product was sold with the serial number 74J1601025.
Inspect the fill port connector for cracks or leaks. If present, stop using the pump immediately.
The pump may have cracks in the fill port connector that could cause leaks, potentially reducing pain relief and requiring extra medication. However, the risk is low if the leak is detected early.
Check for the product code MC0050XLSK5 CP on the pump. The pump model is AF 550 x 5ML/H 6" CATH, 4.5" IN, and it was sold with the serial number 74J1601025.
Stop using the pump immediately and contact Arrow International for a replacement or repair.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0945-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0945-2019 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.
