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# BodyGuard Infusion Sets Recalled
- URL: https://www.fdaweb.com/bodyguard-infusion-sets-recalled/
- Published: 2020-03-18T12:00:00.000Z
- Updated: 2026-09-14T16:07:56.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5146356

CME America has recalled its BodyGuard Microset Infusion Sets due to potential medication flow restrictions. Certain sets (catalog number A120-003XYVA) have an extended section of tubing longer than standard lengths, which can restrict medication flow to the pumping chamber of the infusion pump, according to a recall notice. (XXINSERT LINKXX) “This restriction may result in under-infusion of the therapy,” it says. CME America says it has received three complaints of under-infusion, but no injuries or deaths have been reported. The device delivers fluids or medications into a patient’s body in controlled amounts.