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All product recalls associated with GE Healthcare.
Total Recalls
1000
Past Year
426
Class I (Serious)
54
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 systems do not contain a certification label on the C2 Cabinet (Beam-limiting control).
During ExacTrac Robotics installation on the Varian Exact Couch, the couch height position indication is re-calibrated to read out the correct positions. This re-calibration could cause the eventual failure of the vertical lift mechanism of the couch, which might result in patient injury or death.
Misbranding-The product labeling (label and insert) is misbranded in that the product does not comply with the labeling requirements for an Analyte Specific Reagent (ASR).
To provide the 3.0T MRI systems users with the 8-channel brain coil the proper coil weighting software. The proper coil weighting factors for the eight-channel brain coil were not included in the software.
Labeling; failure to properly label per 21 CFR 1010.2 and 1010.3 -The Operator Console of the Proteus XR/a General Purpose Radiographic Systems were not properly labeled.
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
Weld defect- the weld between the post body and the screw was not properly formed and can fail, even when minimal force is used.
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Proteus XR/a Table while moving the tabletop with the thumb placed over its edge and fingers underneath
The recall involves two models of tree stands: the Ameristep Patriot Hang-On Tree Stand has model number 7300, and the Outfitter Hang-On Tree Stand has model number 7310. These products are fixed-position, strap-on tree stands. The UPC number of the model 7300 is 769524703001. The UPC number of model 7310 is 769524703100. The model number and UPC are not written on the tree stands, but can be found on the packaging.
Systems are non-compliant with Federal Performance Standard Title 21, Code of Federal Regulation (CFR), 1020.32(a)(1) in that the systems allow the production of x-rays when the primary protective barrier is not in position to intercept the entire cross section of the useful beam
The recalled bracelets and necklaces are gold or silver with charms. The charms include a yellow painted metal shirt with "Viva La Juicy" printed on the front, a cheerleader's megaphone with the word "Juicy," a green heart with "Juicy Couture," a black dog, the letter "J," and a purple flower. The jewelry is sold in a pink box with "Juicy Couture" and "Made with Love G&P" printed on the top. Style numbers YJRU0722, YJRU0723, YJR0724 and YJRU0538 are included in this recall. The style number is printed on a white sticker on the bottom of the pink jewelry box.
The two metal frame slingshots being recalled are the Daisy Models ERG-100 and ERG-300, marketed under the name "The Natural." The model number is written on the packaging. These slingshots have an offset fork design, a sling made of bright green tubing with a black leather ammunition pouch and small balls inside the tubing where it connects to the frame. Both models have black plastic handles. The smaller ERG-100 model has the words "Powerline Daisy Mfg. Rogers, AR" on the handle, while the same words are found on the adjustable wrist brace of the larger ERG-300 model. This voluntary recall does not apply to Daisy's Powerline Slingshots models F16, B52 and P51, which have yellow tubing.
No documentation to support shelf life/sterility
The recalled exercise benches are free-standing and typically used for free weight workouts. They have white, gray, or black steel bases, with a black vinyl bench seat and backrest. The Hoist "5-Position Fold-Up Bench," "Folding Flat Bench," and "Folding Ab-Crunch Bench" are included in this recall. Although the bench names and model numbers do not appear on the benches, the serial number is located on a white sticker behind the seat of the bench. Only benches with certain serial numbers are included in this recall. Name of Product Model Number Hoist "5-Position Fold-Up Bench" HF-140 HF-142 BodyGear by Hoist "5-Position Fold-Up Bench" BG-141 BG-143 Hoist "Folding Flat Bench" HF-4163 Hoist "Folding Ab-Crunch Bench" HF-4262
During forward advancement, the user may experience increased resistance and may exhibit jump-effect, and this could result in increase in procedure time, or vessel injury, including perforation.
There is the possibility of a seal void in the Probe Plus packaging which may have compromised the sterility of the device.