Loading...
Loading...
All product recalls associated with GE Healthcare.
Total Recalls
1000
Past Year
421
Class I (Serious)
53
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
A software issue that may result in misregistration of functional and anatomical images associated with the 3.0T BrainwaveRT fMRI Application on the 3.0T Signa HDx scanner.
Unnecessary operator exposure; X-ray machine may allow unwanted x-ray exposure to the operator.
Aortic Length over-estimated: incorrect measurements when using the Aorta analysis protocol or customized protocols. Until a new software version is installed the aorta analysis protocol or the customized protocols for an aneurysm should NOT BE USED.
Results and gates could be mismatched if you utilize the undo function to undo a gate that was deleted.
Inaccurate guidelines: The BE9C is an optional, small radius Bi-planar convex probe intended for use with the LOGIQ 3 Expert system in Urology application. An attempt by the user to activate the biopsy guidelines while this probe is in use will cause incorrect guidelines to be displayed on the image. The incorrect guidelines are recognized by their orientation that is left/right reversed from t
Necessary certification labels are missing from the x-ray contol.
Necessary certification labels are missing from the x-ray contol.
The recall involves the 2007 Raleigh Cadent 1.0, Cadent 2.0 and Cadent Carbon bicycle models with carbon forks. "Raleigh" is printed on the down tube of the bicycle, and the model name is printed on the top tube.
Design Problems Including: 1) Hot Brake (Longitudinal Overheating) potential risk of burns 2) Brake Locks and Sudden Releases 3) Emergency Stop Circuit Button; open instead of closed 4) Longitudinal Brakes Release does not engage properly 5) Tilting Movement causing tabletop to slide; may cause risk of pinched fingers to patient and/or operator 6) Lodging Pins on floor Uncovered; may cause potenti
Inaccurate cassette size display reading/ Inaccurate mAs reading: 1. When the device is in PBL mode and a larger film cassette is inserted into the table Bucky (replacing a smaller cassette) after a protocol is selected on the console, the collimator will not adjust to the larger cassette size. The collimator stays at the original smaller cassette size and allows the operator to take an exposure.
Potential for dialysate leaks from the cartridge during treatment.
This recall involves 190 Radial Brake Master Cylinders used on off-road motorcycles. The brake cylinders have an "A" or "B" code on the underside of the lever's pivot bolt. The Magura logo is printed on the cylinder. Brake cylinders without the "A" or "B" markings are not included in this recall.
Mislabeling: Catheters were found to be mislabeled (90 cm labeled devices actually contains 100 cm length catheter)
When a spectrum of a Pulsed Wave Doppler shows an angle correction unequal to 0 is reloaded from the archive or the image is sent to a DICOM station, this angle correction is mistakenly disregarded resulting in an underestimation of the flow velocities.
The Air Kerma Rate displayed value and cumulative air kerma displayed value could exceed the allowable error under certain imaging conditions.
The Air Kerma Rate displayed value and cumulative air kerma displayed value could exceed the allowable error under certain imaging conditions.
The recall involves both commercial and residential model Cummins Power Generation gaseous-fueled stationary generator sets (fueled by propane or natural gas). They have the following model numbers listed on the generator nameplate which is located at the front base of the unit: commercial models GGDB, GGMA/B/C, and GNAA/B/C, and residential models RS15000, RS20000, and RS30000. These units also have serial number A050734102 through L068998479 and "Cummins Power Generation" listed on the generator nameplate.
Mislabeling: Product is labeled with the wrong expiration date: 2009-12. The correct expiration date is 2008-12.
Reduced Shock- the device may deliver 100 Joule (J) to a patient, which is less than the recommended factory minimum default setting of 200 J.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.