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 might have cracks in the fill port connector. If these cracks leak, the pump may not deliver enough pain medication, requiring extra doses.
Cracks in the fill port connector can cause leaks during use. If undetected, leaks may reduce medication delivery, leading to less pain relief than intended and potentially requiring additional pain medication.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management. Those with the specific product codes listed are most at risk.
Check for the product codes: 74A1801899, 74H1602701, 74B1700146, 74L1700201, or 74B1700921. These pumps were sold with the product name 'Arrow AutoFuser Disposable Pain Control Pump'.
Inspect the fill port connector for cracks or leaks when filling the pump.
74A1801899, 74H1602701, 74B1700146, 74L1700201, and 74B1700921.
Possible cracks in the fill port connector may cause leaks, leading to reduced pain medication delivery and the need for extra pain medication.
Check for leaks in the fill port connector. If leaks are found, contact Arrow for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0944-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0944-2019 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.
