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General Electric Med Systems LLC

General Electric Med Systems LLC Recalls

All product recalls associated with General Electric Med Systems LLC.

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Recall Summary

Total Recalls

1000

Past Year

620

Class I (Serious)

Most Recent

Dec 2025

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.

Showing 10501–10520 of 10937 recalls

General Electric Med Systems LLC: Emission Computed Tomography System. Including Model num...

GE Healthcare received reports of intermittent low ejection fraction (EF) results for MUGA (multi-gated acquisitions) studies on Millennium VG systems. This issue can occasionally lead to distortions in the volume curve in some MUGA studies, and result in calculated EF values lower (never higher) than actual values. A low EF value could lead to a physician decision to stop needed treatment.

FDASep 3, 2004Nationwide• General Electric Med Systems LLC

Fisher Diagnostic, A Company of Fisher Scientific LLC: Pacific Hemostasis brand SickleScreen Sickling Hemoglobin...

Defective reaction vials from an in vitro diagnostic test kit may cause positive patient samples to be interpreted as false negatives.

FDASep 3, 2004Nationwide• Fisher Diagnostic, A Company of Fisher Scientific LLC

Medical Industries America Inc: RemRest Non-Invasive Continuous Positive Airway Pressure ...

Units could show an error code and stop functioning.

1...524 525526527 528...547

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FDASep 3, 2004CO, FL, IL +9 more• Medical Industries America Inc

General Electric Med Systems LLC: LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313...

The Estimated Fetal Weight (EFW) result will be incorrect if the operator fails to perform the 'end exam' or new patient registration step before starting an EFW measurement procedure on the next patient.

FDASep 2, 2004Nationwide• General Electric Med Systems LLC

BC Inflators (Pelagic) – Potential Safety Issue (2004)

The recall includes Oceanic-brand Reliant BC inflators and AERIS-brand AW3 BC inflators. The Oceanic Reliant-type inflators have three flow-through holes in the hand grip of the lower inflator mechanism. The AERIS AW3 inflator has one flow-through hole in the hand grip of the lower inflator mechanism.

CPSCSep 2, 2004Nationwide• Pelagic Pressure Systems, of San Leandro, Calif.

General Electric Med Systems LLC: LOCIQ Book System models: 2399921, 2399923, 2349933, 234...

FDASep 2, 2004Nationwide• General Electric Med Systems LLC

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 4 inch diameter (smal...

The internal ribbon cable may loosen from the roller pump display board, resulting in loss of local control and/or local display.

FDASep 1, 2004Nationwide• Terumo Cardiovascular Systems Corp

Big V Maternity Pillows (Theraline) – Product Safety Risk (2004)

The pillows have a blue or peach-colored print fabric showing yellow moons, hearts and stars, or tan and blue teddy bears. The log-shaped pillows measure about 5 feet in length. "THERALINE," "THE BIG V" and "Finest Micropearl Filling" are written on a fabric tag sewn on the pillow.

CPSCSep 1, 2004Nationwide• Theraline Inc., of Wendell, Mass.

Dade Behring Inc. Rte 896, Glasgow Business Community: DispoSystem for BCT System.Model number OVFR03. Multipurp...

APTT determinations when using affected rotors may lead to incorrectly shortened times

FDAAug 27, 2004Nationwide• Dade Behring Inc. Rte 896, Glasgow Business Community

Cooking Ranges (Whirlpool) – Potential Malfunction (2004)

The recall involves Whirlpool and KitchenAid brand freestanding ranges, double ovens, and oven-microwave combination products with the following model and serial numbers: Brand Product Model Numbers Serial Number Range Whirlpool Oven-microwave combination GSC XR15 - XR25 Whirlpool Double wall oven RBD XR15 - XR25 KitchenAid Oven-microwave combination KEHC KEMC XR15 - XR25 KitchenAid Electric free standing range KERA2 KERI2 RR15 - RR25 The model and serial numbers are located on a label inside the door of the units.

CPSCAug 26, 2004Nationwide• Whirlpool Corp., of Benton Harbor, Mich.

Toshiba American Med Sys Inc: Magnetic Resonance Imaging Systems, under the following n...

Software defect causes patient identification number to be truncated.

FDAAug 24, 2004Nationwide• Toshiba American Med Sys Inc

Becton Dickinson & Company: BD Vacutainer Partial Draw serum tubes (with or without g...

"Please be aware that this is not a new recall. This recall was initially classified in 2005 (Z-0052-05). The firm has taken action; but, due to administrative issues additional products are now being classified by the agency". There is an apparent bias in the determination of Total T3, Total T4, HBsAg, Folate BA, VB 12, BR, FSH and Cortisol hormones used to determine thyroid disease states, and a

FDAAug 20, 2004Nationwide• Becton Dickinson & Company

Philips Medical Systems Sales & Service Region No. America: NT Intera Magnetic Resonance Image System

Fire/Burn Risk

Potential for patient burn

FDAAug 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Becton Dickinson & Company: BD Vacutainer Microtainer Serum tubes (with or without gel).

FDAAug 20, 2004Nationwide• Becton Dickinson & Company

Becton Dickinson & Company: BD Vactuainer SST glass and plastic tubes.

"Please be aware tht this not a new recall. The firm has taken action; but, due to administrative issues additional products are now being classified by the agency". There is an apparent bias in the determination of Total T3, Total T4, HBsAg, Folate BA, VB 12, BR, FSH and Cortisol hormones used to determine thyroid disease states, and adrenal gland function. The immunoassay results are high when

FDAAug 20, 2004Nationwide• Becton Dickinson & Company

Toddler Bicycle Helmets (PTI Sports) – Safety Concern (2004)

These Schwinn-brand Toddler Bicycle Helmets have "SCHWINN" written on the back of the helmets. A white label inside the helmets reads, "Lot# 791913." This number is followed by a date from "12-01-03" through "5-15-04." This label also contains the model number SK103, SK107 or SK108.

CPSCAug 19, 2004Nationwide• PTI Sports Inc., of Rancho Cucamonga, Calif.

Windsor Dinette Chair (American Signature) – Structural Defect (2004)

This recall involves "Windsor" style arm chairs. The chairs measure 40 inches high by 21 inches wide. Made of black wood, the chairs have 9 metal spindles across the rounded back.

CPSCAug 18, 2004Nationwide• American Signature Inc., of Columbus, Ohio

Kitchen Krumblers Apple Candle (Mostly Memories) – Potential Hazard (2004)

Fire/Burn Risk

The scented candle is housed in a clear glass holder and has a crumbled appearance with color variations. It contains slices of dried apple and cinnamon sticks in the wax. The candle is 3 inches in diameter and 3.5 inches high. "Kitchen Krumblers" is labeled at the base of the candle. The candle was sold separately or in a set with another candle not involved in this recall.

CPSCAug 18, 2004Nationwide• Mostly Memories Inc., of Ozark, Mo.

Rackmount UPS (Belkin) – Power Supply Risk (2004)

The recalled Belkin OmniGuard Rackmount UPS units are used to provide voltage regulation, surge suppression, and back-up power for electronic equipment. The Belkin OmniGuard Rackmount UPS units are black with a silver/gray panel on the front. Recalled units are the OmniGuard 1100 (Model no. F6C110-RKM-2U), OmniGuard 1500 (Model no. F6C150- RKM-2U), OmniGuard 2300 (Model no. F6C230-RKM-2U), and OmniGuard 3200 (Model no. F6C320-RKM-3U). The model number and model type can be found on a label on the rear of the unit.

CPSCAug 17, 2004Nationwide• Belkin Corp., of Compton, Calif.

10,000 Lux Light Box (OTT-LITE) – Safety Concern (2004)

Fire/Burn Risk

The recalled "10,000 Lux Light Box" produces light to simulate natural sunlight. The units, which are white with a translucent hinged door, measure 24 inches high, 12 ½ inches wide, and 3 ¾ inches deep. Some of the recalled light boxes may have a small label on the top of the unit with the name "Nu-Yu Light." Only the "10,000 Lux Light Box" sold by Natural Options is recalled.

CPSCAug 11, 2004Nationwide• OTT-LITE Technology of Tampa, Florida