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 when filling the pump. If undetected, this could lead to reduced drug delivery and less pain relief than prescribed, possibly requiring extra medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps are affected. Those with the specific product codes listed are most at risk.
Check for the product codes listed in the recall notice: 74A1801376, 74G1702799, 74A1801900, and other codes provided. These pumps were sold with the specific product code MVBXL-CPNB.
Inspect the fill port connector for cracks or leaks when filling the pump.
Reach out to Arrow International for guidance on next steps if leaks are found.
The recall is for possible cracks in the fill port connector that could cause leaks, leading to reduced pain relief and needing extra medication.
The affected product codes include 74A1801376, 74G1702799, 74A1801900, and other codes listed in the recall notice.
No, but you should check for leaks and contact Arrow if you find any issues.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0940-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0940-2019 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.
