All Recalls

Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.

Automated external defibrillators were shipped in their test configuration so there is a potential to have incorrect language, and CPR duration resulting in the device prompting users to perform CPR for 5-seconds, and it could analyze heart rhythm and instruct users to deliver a shock every 5-seconds if a shockable heart rhythm is detected, potentially leading to no therapy or delayed therapy.

GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling.

GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling.

While performing a fluoroscopy examination, there is a potential that the Radio Fluoroscopy (RF) viewer will also display a previous patient's radiography images. If the issue occurs, there will be differences in image content, image format and image size.

The firm has become aware of a sudden increase in complaints for three associated lots. Performance issues may lead to impaired embryo development prior to the blastocyst stage.

Due to a trend in false positive Candida tropicalis results on blood culture panel when using certain BD BACTEC vial mediums

The laptop AC adapters can overheat and spark, posing burn and fire hazards.

The portable fuel bottles do not meet the child-resistant requirements for closures under the Children's Gasoline Burn Prevention Act (CGBPA). The closure for the products is not child-resistant, posing a risk of burn and poisoning to children. The 530mL BRS bottle was manufactured after the Portable Fuel Container Safety Act (PFCSA) became effective and lacks a flame mitigation device, posing a flash fire hazard.

The control panel (user interface) on the ranges can detach from the unit, posing electrical shock and electrocution hazards.

The recalled greenhouses can overheat, posing a fire hazard resulting in property damage and injury.

The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.

The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.

Foreign manufacturer of recalled product listed on IA #99-37 due to having no filed scheduled process.

The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.

Product contains undeclared soy lecithin.

The food was not held at an appropriate temperature. The holding temperature could affect spoilage and potentially support pathogen growth.