Arrow recalls disposable pain control pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief. Affected units include specific product codes sold from 2020-2021.
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 pumps that may have cracks in the fill port connector. These cracks could cause leaks during use, potentially reducing pain relief and requiring extra medication. This recall affects users who need consistent pain management.
The fill port connector may crack, causing leaks when the pump is being filled. If the leak isn't noticed, the pump might deliver less medication than intended, leading to less pain relief than prescribed and possibly requiring additional pain medication.
Users of Arrow AutoFuser disposable pain pumps with product code MVBX60XL CPNB are affected. Patients relying on these pumps for pain management are most at risk of reduced medication effectiveness.
Check for product code MVBX60XL CPNB on the pump's label. These pumps were sold from 2020-2021 with the model name 'Arrow AutoFuser Disposable Pain Control Pump'.
Inspect the fill port connector for cracks or signs of leakage when filling the pump.
The recall is for possible cracks in the fill port connector that could cause leaks, potentially reducing pain relief and requiring extra medication.
The official recall notice does not specify a remedy or action steps beyond checking for leaks. Contact Arrow International for further guidance.
The recall indicates a low risk of reduced pain relief due to possible leaks, but the official notice does not mention serious injury risks.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0956-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0956-2019 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.
