Arrow recalls disposable pain pumps with possible cracks in fill port connectors that may cause leaks, leading to reduced pain relief. Affected units may need additional pain 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 recalls disposable pain control pumps that could have cracks in the fill port connector. If leaks occur during use, patients might get less pain relief than prescribed and need extra medication.
Cracks in the fill port connector can cause leaks during medication filling. If undetected, leaks may reduce drug delivery, leading to less pain relief than prescribed and possibly requiring extra pain medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management. Those with the specific product code MVBT30XL CPNB are most at risk.
Check for the product code MVBT30XL CPNB on the pump. The pump is sold under the brand name Arrow AutoFuser Disposable Pain Control Pump.
Inspect the fill port connector for cracks or leaks when filling the pump.
The pump may have cracks that cause leaks, potentially reducing pain relief. However, the recall does not indicate immediate danger to health.
The recall does not specify a remedy, so check for leaks and contact Arrow if you find cracks.
Look for the product code MVBT30XL CPNB on the pump, which is sold under the Arrow AutoFuser Disposable Pain Control Pump brand.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0955-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0955-2019 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.
