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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.
Failure to properly pre-indicate the technique factors to be used during a patient scan.
Failure to properly pre-indicate the technique factors to be used during a patient scan.
LRF models were sold to non-DoD customers prior to certification and reporting as required in Title 21 of the Code of Federal Regulations, Subchapter J, Parts 1000 - 1050 (21 CFR 1000 - 1050). A filter defect allows transmission of laser energy such that the affected LRF would be Class 3B laser product, however the product is reported to CDRH as a Class I product.
Review by firm of Philips EasyVision MM workstations found that to assure compliance with 21 CFR 900.12(c)(5) corrected software was needed so that all sites are in compliance.
Instruction for use incorrect: There are no statements or warning on labels or Instructions for Use that 8, 9 and 10 mm diameter MRS Cemented Stems are indicated only for use in the GMRS Proximal Tibial and Distal Femoral Components.
A manufacturing defect may prevent adequate sterilization of the entire device.
A manufacturing defect may prevent adequate sterilization of the entire device.
A manufacturing defect may prevent adequate sterilization of the entire device.
The product is mislabeled, in that, zero/low controls were mislabeled as medium/high, and the medium/high controls were labeled zero/low.
A manufacturing defect may prevent adequate sterilization of the entire device.
The R1 reagent has microbial contamination.
This recall involves Stabilicers Lite cleats with model number BNX9. The cleats are worn over footwear for traction in winter walking conditions. The recalled cleats were sold in blue, orange, and pink. Black Stabilicers Lite cleats are not included in this recall. The cleats were sold in sizes small through extra large. The name Stabilicers Lite appears in raised letters on the underside of the harness.
A software error in the TumorLoc software was discovered upon receipt of a customer complaint. There is the potential for data to be lost during reconstruction of images in which slices can either be discarded, or interleaved based upon their series ID.
The recall was initiated after Alphatec Spine received a complaint on the ILLICO Posterior Thoracolumbar access retractor. It was reported that one of the retractor arms in the retractor broke during surgery.
The recalling firm manufactured and distributed peanut products which contained peanuts and/or peanut butter which they received from there bulk peanut supplier, Peanut Corporation of America (PCA). Peanuts and peanut products produced by PCA have been implicated in a recent outbreak of salmonellosis and these product may be contaminated with Salmonella Typhimurium.
The recalled winter gloves are black-colored and have a battery-powered heating element. The gloves included in the recall are style number 77000 (men's) in sizes S, M, L, XL, and style number 77010 (women's) in sizes S, M, L. The product name is printed on the inside cuff of the left glove.
The recalling firm manufactured and distributed peanut products which contained peanuts and/or peanut butter which they received from there bulk peanut supplier, Peanut Corporation of America (PCA). Peanuts and peanut products produced by PCA have been implicated in a recent outbreak of salmonellosis and these product may be contaminated with Salmonella Typhimurium.
The recalled canopies involve the "Home Sweet Playhome" model made of 100% cotton gingham fabric draped from a bamboo hoop which is suspended from the ceiling to create a cylindrical play space measuring 36 inches wide and 9 feet tall. The canopies have an open bottom, a "door" and three multi-paned "windows." They were sold in blue and pink. "Home Sweet Playhome" canopies sold after October 2005 are not included in this recall. "The Land of Nod" is printed on a woven label on the canopy.
Bur guards were distributed without an expiration date, and if they are used after they have expired it could result in the patient or operating room staff experiencing a burn or laceration.
These wall mounts are used with flat screen LCD televisions. The recalled wall mounts are INIT models NT-TVM103 and NT-TVM104. The model numbers can be found on the UL sticker on the television interface.