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 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. These cracks could cause leaks during use, potentially reducing pain relief and requiring additional medication. This affects patients using the pumps for pain management.
The fill port connector may crack, causing leaks during medication filling. If undetected, leaks could reduce drug delivery to patients, leading to less pain relief than prescribed and possibly requiring extra pain medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management are most at risk. The recall applies to specific product codes sold between 2020 and 2023.
Check for product codes: MVAXL2Y CPNB, 74A1600493 through 74K1601957. These pumps were sold by Arrow International Inc. between 2020 and 2023.
Inspect the fill port connector for cracks or leaks when filling the pump.
Reach out to Arrow International Inc. for guidance on next steps if leaks are found.
The pumps may have cracks in the fill port connector that cause leaks, potentially reducing pain relief and requiring additional medication.
Check the fill port connector for cracks and contact Arrow International Inc. for guidance.
Yes, the affected product codes are MVAXL2Y CPNB and the serial numbers listed in the recall notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0952-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0952-2019 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.
