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# CME BodyGuard Infusion Pump Recalled
- URL: https://www.fdaweb.com/cme-bodyguard-infusion-pump-recalled/
- Published: 2020-03-31T12:00:00.000Z
- Updated: 2026-09-14T16:09:26.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5146458

CME America has recalled the BodyGuard Infusion Pump Systems because they may under or over infuse medications. The reason for the infusion errors is not known, a recall [notice ](https://www.fda.gov/medical-devices/medical-device-recalls/cme-america-recalls-bodyguard-infusion-pump-system-due-risk-over-and-under-infusion?ref=fdaweb.com)says. Using an affected infusion pump may cause serious adverse health consequences including death, it says. To date, there have been 158 complaints about the infusion issue. The device is intended to deliver fluids and medications into a patient’s body in controlled amounts.