Arrow recalls disposable pain control pumps with possible fill port cracks causing leaks. Leaks may reduce pain relief and require extra medication. Check product codes for affected units.
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, leading to reduced pain relief and the need for extra medication. Affected units might require a different pump to avoid medication delays.
Cracks in the fill port connector can cause leaks when filling the pump. If undetected, leaks may reduce drug delivery, leading to less pain relief than prescribed 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 product codes: 74A1701422, 74G1702788, 74B1700142, 74M1600770, 74C1701810, 74M1601742, 74G1702049, 74M1602233. The product is an Arrow AutoFuser Disposable Pain Control Pump.
Identify if your pump has any of the listed product codes: 74A1701422, 74G1702788, 74B1700142, 74M1600770, 74C1701810, 74M1601742, 74G1702049, 74M1602233.
The pump may have cracks in the fill port connector that can cause leaks, potentially reducing pain relief and requiring extra medication.
Check if your pump has any of the listed product codes. If it does, contact Arrow for further instructions.
The recall addresses potential leaks that could reduce pain relief, but there is no mention of serious injury risks in the official notice.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0946-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0946-2019 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.
