Arrow recalls disposable pain pumps with possible cracks in fill port connectors that may leak, leading to reduced pain relief and needing extra medication. Affected units have specific product codes.
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 recalls disposable pain control pumps that may have cracks in the fill port connector, causing leaks. If undetected, leaks could reduce pain medication delivery, requiring extra painkillers.
Cracks in the fill port connector can cause leaks during use. If the leak isn't noticed while filling the pump, less medication reaches the patient, potentially needing extra painkillers.
People using Arrow AutoFuser Disposable Pain Control Pumps for pain management. Those with medical conditions requiring precise pain control are at higher risk.
Check for product code MT8015XL CPNB or the specific model name 'AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP'. These pumps were sold with the serial number 74B1602449.
Look for cracks in the fill port connector that might cause leaks during use.
The recall states possible leaks could reduce pain medication delivery, but no serious injury is mentioned.
The recall does not specify a stop-use instruction; users can check for leaks and continue if no issues are found.
Check for product code MT8015XL CPNB or model name 'AF 550 x 8ML/HR 2ML 15LO CPNBMT8015XL CP' with serial number 74B1602449.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0950-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0950-2019 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.
