Optum recalls Nimbus II Plus infusion pumps (model AAA-00170) due to potential battery failure, occlusion, system errors, and drug leakage. Affected units have specific lot/serial numbers listed in the recall.
Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being removed the from the market due to multiple potential failure modes, including battery failure, upstream occlusion, system errors, drug product leakage, high or low flow rate, or damaged pump housing.
Optum is recalling Nimbus II Plus ambulatory infusion pumps (model AAA-00170) because they can fail in multiple ways, including battery issues, blockages, system errors, and drug leaks. This poses a risk of serious injury or death for users who rely on these pumps for medical treatment.
The pump can fail in multiple ways, including battery failure, blockages in the system, software errors, drug leaks, incorrect flow rates, or damage to the pump housing. These failures could lead to serious injury or death if the pump stops working during critical medical treatment.
People using the Optum Nimbus II Plus ambulatory infusion pump for medical treatment are affected. Those with the specific lot and serial numbers listed in the recall are most at risk.
Check the lot number and serial number on your pump. Affected units have specific combinations listed in the recall, such as Lot 302604 with Serial NIMBP702231 or Lot 318050 with Serial NIMBP715656.
If you have the recalled model with the listed lot and serial numbers, stop using the pump right away to prevent potential failure.
The recalled model is Optum Nimbus II Plus, model number AAA-00170.
Check the lot number and serial number on your pump. Affected units have specific combinations listed in the recall, such as Lot 302604 with Serial NIMBP702231.
Stop using the pump immediately and contact OptumHealth Care Solutions for further instructions.
We’ve drafted a message you can send Optum to request your refund or repair — edit it as you like.
Subject: Recall Z-1811-2024 — Optum Optum Hello, I own a Optum that is covered by recall Z-1811-2024 from Optum. 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.
