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All product recalls associated with GE Healthcare.
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
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.
The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
Maximo II VR ICD, DR ICD and CRT-D inadvertently include the Capture Management algorithm (Atrial/Right Ventricular/Left Ventricular Capture management). The Capture management algorithm monitors daily pacing thresholds and may increase or decrease pacing amplitudes in response to patients' needs. Although the algorithm is operating correctly, it is not accessible to the clinician for reprogramm
Failure to restrain: This recall was initiated after a complaint was received by the firm regarding a Posey 2217SL unit indicating that a patient was able to pull the rivet or washer through the synthetic leather allowing the patient to have freedom of arm movement. A second complaint was received indicating that a patient was able to tear the strap at the adjustment notch on a Posey 221 7SL unit
The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.
Maximo II VR ICD, DR ICD and CRT-D inadvertently include the Capture Management algorithm (Atrial/Right Ventricular/Left Ventricular Capture management). The Capture management algorithm monitors daily pacing thresholds and may increase or decrease pacing amplitudes in response to patients' needs. Although the algorithm is operating correctly, it is not accessible to the clinician for reprogramm
The Reebok Studio Cycle is an upright exercise bike used primarily in fitness centers and other institutional settings. The recalled bicycle is black with silver cranks. The unit has an internal belt drive. The base of the bicycle is a single piece that is welded to the frame. The legs are two straight horizontal bars with rounded edges. There is a logo located on the side of the exercise cycle that shows a person riding a bicycle.
The product is mislabeled, as the validation for the previous sterilization parameters cannot be replicated. The currently validated sterilization parameter is a minium of 24 minutes prevacuum.
The recalled Dirt Devil Turbo Tool/Power Brush attachment was sold as an accessory with the following Dirt Devil vacuum models. Only vacuum tool accessories with date codes J7060 through J7365 and have a C-clip connector are included in this recall. The date code is located on the underside of the vacuum accessory. The Turbo Tool/Power Brush tools are about 6 ½ inches long by about 5 inches wide and come in a variety of colors that match the color of the vacuum. The housing of the tool was made in clear, red, green, or light blue with clear, light blue, dark blue, red, purple, or black turbine fans with matching brush rolls. Dirt Devil Vacuum Models Reaction Purpose for Pets Ultra Swivel Glide M110000 M140000 M086020 M110000HD M140000CA M110001B M110002 Envision Wide Glide Swerve M110003 M086700WCA M086030 M110006 M086710 M086030CA M110008 M110008CA Action Upright Royal Commercial M110009 M110020CAB RY6100
The recalled Walther air cylinders for air pistols are aluminum and involve model 2/WALTHER 85 cm3, with the imprinted test date between 6 00 and 6 01 2000/2001 located on the end of the cylinder.
Software: If Weight Limits edited, values will return to default values that were deleted
The recalled fixture is a ceiling-mounted downlight. Model number LV3R is included in this recall and is printed on a UL label inside the light's housing.
Potential for module to fail to obtain a NIBP reading on hypertension patients.
BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have
BD Diagnostics GeneOhm (BDDG) initiated the recall after they identified that the product has the potential to identify a patient as falsely positive for colonization with methicillin resistant Staphylococcus aureus. The potential health hazard related to a false positive result from this assay would be that a patient may be misclassified as having MRSA colonization when in fact they do not have
Telemetry Modules are failing to alarm for low heart rate and asystole.
Local pump controls including start/stop button, select button and manual button may not function.
The Alternate Site Cap was not included in the package as indicated on the labeling.
The units may exhibit blank or distorted displays, loss of local control and/or may have local control knobs that are difficult to use.