Arrow recalls disposable pain control pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief and potential need for additional 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 extra medication.
Cracks in the fill port connector may cause leaks when filling the pump. If undetected, leaks could reduce drug delivery, leading to less pain relief than prescribed and possibly requiring additional medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management. Those with the specific product codes listed are most at risk.
Check for the product code MT8015XLYK10 CP on the pump. The specific product codes listed in the recall include 74A1701382, 74H1701147, and other codes.
Inspect the fill port connector for cracks or leaks when filling the pump.
Arrow AutoFuser Disposable Pain Control Pumps with product code MT8015XLYK10 CP.
Leaks may reduce drug delivery, leading to less pain relief than prescribed and possibly requiring additional medication.
Check for the product code MT8015XLYK10 CP on the pump, or look for the listed codes such as 74A1701382.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0951-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0951-2019 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.
