Arrow recalls disposable pain pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief. Affected units include specific product codes and serial numbers.
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. If these cracks cause leaks, patients could get less pain relief than prescribed, requiring extra medication.
Cracks in the fill port connector can cause leaks during use. If the leak is not noticed while filling the pump, patients might receive less pain medication than prescribed, requiring additional pain relief.
Patients using Arrow AutoFuser Disposable Pain Control Pumps with specific product codes and serial numbers are affected. Those with the pumps already in use are most at risk.
Check for product code MVBX30XLCPNB or serial numbers 74M1500647 and 74G1702789 on the pump packaging or label.
Inspect the fill port connector for cracks or leaks when filling the pump.
Arrow AutoFuser Disposable Pain Control Pumps with product code MVBX30XLCPNB and serial numbers 74M1500647 or 74G1702789.
Possible cracks in the fill port connector may cause leaks, leading to reduced pain relief and the need for additional medication.
No, but check for leaks before use. If leaks are found, contact Arrow for assistance.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0953-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0953-2019 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.
