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 pain medication.
The fill port connector may crack, causing leaks when the pump is being filled. If the leak goes unnoticed, the patient may receive less pain medication than prescribed, requiring additional pain relief.
Patients using Arrow AutoFuser Disposable Pain Control Pumps for pain management are most at risk if the pump has a crack in the fill port connector that causes leaks.
Look for the product name 'Arrow AutoFuser Disposable Pain Control Pump' with model number MT5060XLYK5 CP. The pumps were sold with serial numbers 74F1700794, 74J1700676, and 74J1700190.
Inspect the fill port connector for cracks or leaks when filling the pump.
The pump may have cracks in the fill port connector that could cause leaks, leading to reduced pain relief. However, the risk is low and not all pumps are affected.
Check the product name and model number on the pump. Recalled units have the model MT5060XLYK5 CP and serial numbers 74F1700794, 74J1700676, or 74J1700190.
If you notice a leak while filling the pump, stop using it and contact Arrow for a replacement.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0943-2019 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0943-2019 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.
