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GE Healthcare, LLC

GE Healthcare, LLC Recalls

All product recalls associated with GE Healthcare, LLC.

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Recall Summary

Total Recalls

1000

Past Year

423

Class I (Serious)

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.

Showing 1481–1500 of 4598 recalls

Optima MR450w (GE Healthcare) – Image Slice Missing Risk (2021)

Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.

FDAAug 26, 2021Nationwide• GE Healthcare, LLC

SIGNA HDxt MR System (GE Healthcare) – Image Slice Missing Risk (2021)

Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.

FDAAug 26, 2021Nationwide• GE Healthcare, LLC

SIGNA Creator/Explorer (GE Healthcare) – Image Slice Missing Risk (2021)

Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.

FDAAug 26, 2021Nationwide• GE Healthcare, LLC

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Betamethasone Dipropionate Lotion (Teligent) – Stability Failure (2021)

Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing

Class IIModerate

FDAAug 23, 2021Nationwide• Teligent Pharma, Inc.

VOLKSWAGEN TAOS (VOLKSWAGEN) – Fuel Line Connector Defect (2021)

Fire/Burn Risk

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Taos vehicles. The underhood fuel supply quick-connector may detach from the fuel supply line causing a fuel leak in the engine compartment.

NHTSAAug 20, 2021Nationwide• VOLKSWAGEN

PALFINGER KNUCKLE BOOM CRANE (PALFINGER) – Base Cracking Risk (2021)

Palfinger, Inc. (Palfinger) is recalling certain Knuckle Boom Cranes, models PW38001, 42001, and 50001. The crane base may crack over time from normal crane use.

NHTSAAug 18, 2021Nationwide• PALFINGER

BRIDGESTONE TURANZA EL440 Tire (BRIDGESTONE) – Sidewall Issue (2021)

Fire/Burn Risk

Bridgestone Americas Tire Operations (Bridgestone) is recalling certain Bridgestone Dueler H/L 422 Ecopia P245/60R18, Dueler H/L Alenza 275/55R20, Ecopia H/L 422 Plus 235/55R20, Turanza EL440 235/60R18, and Firestone Destination LE3 225/65R17 tires with DOT code 2821. These tires may have been manufactured with a pinhole in the outboard side of the tire. As such, these tires fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 139, "New Pneumatic Radial Tires for Light Vehicles."

NHTSAAug 18, 2021Nationwide• BRIDGESTONE

Centricity Universal Viewer (GE Healthcare) – study management error (2021)

A software anomaly exists in the Centricity Universal Viewer study management feature in which study changes are not propagated to either the Centricity Enterprise Archive (EA) or another Vendor Neutral Archive (VNA).

FDAAug 12, 2021AR, IL, ME +5 more• GE Healthcare, LLC

Triple Berry Streusel Cheesecake (Gem City) – Mislabeled Ingredients (2021)

Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with Triple Berry Streusel Cheesecake ingredients and nutrition label. Chocolate Torte and Triple Berry Streusel are both mislabeled with pecans as an ingredient although firm has not used nuts of any kind in its products or the facility since April 2018.

Class IIILow

FDAAug 7, 2021CO, IN, TX• Gem City Fine Foods, LLC

Flourless Chocolate Torte (Gem City) – Mislabeled Ingredients (2021)

Class IIModerate

FDAAug 7, 2021CO, IN, TX• Gem City Fine Foods, LLC

Volkswagen Taos (Volkswagen) – ECU Software Issue (2021)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Taos vehicles equipped with all-wheel drive. The engine control unit (ECU) software may cause a stall when coming to a stop.

NHTSAAug 6, 2021Nationwide• VOLKSWAGEN

Centricity Universal Viewer (GE Healthcare) – Image Sync Failure (2021)

Image acquisition failures and synchronization failure with the Centricity Enterprise Archive

FDAAug 6, 2021AK, AZ, CA +31 more• GE Healthcare, LLC

Volkswagen Atlas (Volkswagen) – Damaged Relays (2021)

Fire/Burn Risk

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Atlas and Atlas Cross Sport vehicles. Damaged relays may have been installed in the engine compartment fuse box, which could inadvertently activate the horn or engine starter.

NHTSAAug 6, 2021Nationwide• VOLKSWAGEN

Centricity PACS-IW (GE Healthcare) – Image Sync Failure (2021)

Image acquisition failures and synchronization failure with the Centricity Enterprise Archive

FDAAug 6, 2021AK, AZ, CA +31 more• GE Healthcare, LLC

AMSORB PLUS Prefilled G-CAN (Armstrong Medical) – Gas Flow Resistance (2021)

Some devices may be associated with high and unexpected resistance to gas flow during clinical use, impacting or preventing adequate ventilation of an anaesthetised patient, which could cause a delay in treatment. Not all defective canisters will be identified by the pre-use test.

FDAAug 5, 2021Nationwide• Armstrong Medical Services Limited NewBridge Road Wattstown Business Park Coleraine Ireland

Volkswagen ID.4 (Volkswagen) – Seat Belt Assembly Issue (2021)

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 ID4 vehicles. Incorrect rear outboard seat belt assemblies without an automatic locking retractor (ALR) function may have been installed, which can prevent the child restraint system from securing properly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection."

NHTSAAug 4, 2021Nationwide• VOLKSWAGEN

Lidocaine Topical Solution (Teligent) – Potency Problem (2021)

Superpotent Drug

Class IHigh

FDAAug 3, 2021Nationwide• Teligent Pharma, Inc.

GE Healthcare, LLC: Flow sensors kept as stand-alone user replaceable spare p...

Laceration Risk

The flow sensors built prior to June 2021 could have damaged tubes with small punctures or cuts that could cause leaks resulting in incorrect anesthesia machine tidal volumes potentially leading to over-delivery of volume to the patient.

FDAAug 2, 2021Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: Flow sensors that may be installed in the following GEHC ...

Laceration Risk

FDAAug 2, 2021Nationwide• GE Healthcare, LLC

Portable Generators (Generac) – Amputation Risk (2021)

This recall involves 6500 watt and 8000 watt Generac portable generators with unit type numbers XT8000E, XT8000EFI, GP6500, GP6500E, GP8000E and HomeLink 6500E portable generators, and DR models PRO 6500M and PRO 6500E portable generators. The generators have gasoline-powered engines that are used to generate electricity for use as backup power. The portable generators have two-wheels and a single, U-shaped, two-grip, flip-up pin-lock handle to help move the generator. Only the generators listed below are included in this recall. The unit type is identified on the front of the product. The model and serial numbers are printed on a label on the product. Consumers can also check specific unit type, model number, and serial number location information at www.generac.com/service-support/product-support-lookup Unit Type Model Number First Serial Number Last Serial Number XT8000E G0064330 G0064331 3000037849 3005569372 G0064340 G0064342 XT8000EFI G0071620 G0071621 3003336356 3006597843 G0071621R GP6500 G0076720 G0076800 G0076800R G0076812 G0076830 G0076830R G0076902 G0076902R G0076903 GP6500E G0076820 G0076820R G0076822 GP8000E G0076731 G0076751 G0076751R G0076761 G0076761R G0076861 G0076861R PRO 6500M GP16505DMN GP16505DMNR PRO 6500E GP16505DEN HomeLink 6500E G0068650 G0068651 G0079960

CPSCJul 29, 2021Nationwide• Generac Power Systems, of Waukesha, Wis.