Arrow recalls disposable pain pumps with possible cracks causing leaks that may reduce pain medication delivery. Affected models include AF 550 x 5ML/HR 2ML 60LO CPNB (product code MT5060XL CPNB).
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, leading to less pain relief than prescribed and potentially requiring extra pain medication.
Cracks in the fill port connector can cause leaks when the pump is being filled. If undetected, leaks may reduce the amount of medication delivered, leading to less pain relief than intended and possibly requiring additional pain medication.
Patients using Arrow AutoFuser disposable pain pumps for pain management are affected. Those with the specific product codes listed are most at risk.
Check for the product code MT5060XL CPNB on the pump. Affected pumps were sold with serial numbers 74A1700874, 74G1702797, 74F1700146, 74H1701106, and 74F1701964.
Inspect the fill port connector for cracks or leaks when filling the pump.
The product code is MT5060XL CPNB.
Check for the product code MT5060XL CPNB and serial numbers 74A1700874, 74G1702797, 74F1700146, 74H1701106, or 74F1701964.
The recall does not require immediate stoppage; check for leaks before continuing use.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0948-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0948-2019 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.
