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All product recalls associated with GE Healthcare.
Total Recalls
1000
Past Year
631
Class I (Serious)
65
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.
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.
Overheating; A portion (balun assembly) of the cable that connects the shoulder coil to the actual MRI unit may malfunction and result in overheating of the balun assembly. The overheating of the balun assembly could result in injury to the patient or operator if either came into contact with the assembly.
The recalled TV Stand measures 23 ¾ inches (h) x 38 ½ inches (w) x 19 ½ inches (d) with a brushed maple finish. The stand has criss-cross, black, wrought-iron legs, a pull-out drawer, and a lower shelf. Model number 400205 and UPC number 42666 01958 are located on the product's carton and instructions.
Method is susceptible to positive interference from endogenous ALT in patient samples.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Units do not comply with the requirement to provide automatic beam limitation within +/- 3 degrees of horizontal, vertical, and perpendicular to the plane of the image receptor during radiographic procedures.
Sterility compromised (package integrity): The primary packaging for a portion of the lot may contain gloves that were not sealed properly.
Peak voltage test result not in acceptable limits.
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.
The BMSI "MicroJack" patient interface electrode connection device used with the EEG monitor systems was found to be mis-wired. A complainant alleged that during depth electrode EEG study of a patient in preparation for brain surgery there was an observation that was perceived as non-logical data output.
The carton label may not reflect the correct size of the acetabular cup.
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.
This recall involves Thermador® Brand built-in single ovens and combination models which have a conventional oven and a microwave. The model numbers of the single ovens are C271B, C301B, SEC271B and SEC301B. The model numbers of the combination models are SEM272B, SEM302B, SEMW272B and SEMW302B. The ovens have date codes between FD8403 and FD8701. The model number and date code can be found on the underside of the control panel.
Incomplete seal on the product pouch; with the seal incomplete, the sterility of the product inside the pouch cannot be guaranteed.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.
Falsified Repair/Test and Inspection records: Pumps submitted for repair or service may not have been properly repaired or serviced before being returned to the customer.