FDASeptember 16, 2019device
BodyGuard Microset REF A120-003XYVA, Sterile EO, Tubing: 150 in. (380 cm), Prime Vol: approx. 8ml Product Usage: The BodyGuard Infusion Pump System is designed to transfer medication and fluids intravenously.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
When using a specific tubing set with infusion pump system, may result in under deliver of fluids.
What to do
FDA enforcement status: Terminated
Brands named
cme americacme
UPCs
00818666020146
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDADigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.2026-05-01
- CPSCAcer America Corporation Recalls Two-Wheeled Folding Electric Due to Risk of Injury from Fall Hazard2026-04-30
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