FDAJuly 1, 2008device
GE Precision MPi is an all-digital multipurpose tilt-C x-ray system, intended for a multitude of diagnostic procedures, including radiology, fluoroscopy, interventional procedures, vascular and non-vascular procedures, and specialized applications including angiographic studies.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi X-ray system may not always boot up as intended and needs to be updated to properly accomplish its intended purpose.
What to do
FDA enforcement status: Terminated
Brands named
regulatory insightregulatory
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDATING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 32024-02-01
- FDAAmericaine, (benzocaine 20%) Benzocaine Topical Anesthetic Spray, Aerosol Can 2 oz (57 G), Dist. by Insight Pharmaceuticals Corp. Tarrytown, NY 10591, USA, A Prestige Consumer Healthcare company. Made in India. NDC 63736-378-02, Can UPC 3 63736 37882 0; Case UPC 1 03 63736 37882 72023-12-21
- FDATING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.2023-11-22
- CPSCRelion Battery Recalls Relion Insight Series Lithium Batteries Due to Thermal Burn and Fire Hazards2023-03-02
- CPSCDouble Insight Recalls Multicookers Due to Fire Hazard; Sold Exclusively at Walmart2018-03-01
- FDAClariVein IC infusion catheter, Model Number: 65-018-E4S Product Usage: The ClariVein IC infusion catheter is indicated for infusion of physician-specified agents into the peripheral vasculature.2017-11-09
- CPSCInstant Pot Pressure Cookers Recalled by Double Insight Due to Shock Hazard (Recall Alert)2015-07-15
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