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. This could cause leaks during use, resulting in less pain relief than prescribed and possibly requiring additional medication.
The fill port connector may crack, causing leaks during medication filling. If undetected, this could lead to reduced drug delivery and less pain relief than prescribed, potentially requiring extra medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management are affected. Those with medical conditions requiring precise pain control are at higher risk.
Check for the product code MT5060XLSK5 CP on the pump. The pumps were sold with specific serial numbers listed in the recall notice.
Inspect the fill port connector for cracks or leaks before use.
The pump may have cracks in the fill port connector that could cause leaks, leading to reduced pain relief and possible need for additional medication.
Check the fill port connector for cracks. If you find a leak, stop using it and contact Arrow for assistance.
The recall does not specify a fix; users should check for leaks and contact Arrow if needed.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0942-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0942-2019 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.
