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GE Medical Systems Information Technologies Inc

GE Medical Systems Information Technologies Inc Recalls

All product recalls associated with GE Medical Systems Information Technologies Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

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 3621–3640 of 21320 recalls

Prucka 3 Amplifiers (GE Medical) – Power Supply Failure (2023)

A diode on the power supply of the Prucka 3 Amplifier used with CardioLab/ComboLab systems could reach elevated temperatures and fail, then power off and become inoperable.

Moderate

FDAAug 8, 2023CA, CO, FL +14 more• GE Medical Systems Information Technologies Inc

Strawberry Mango Sorbet (Real Kosher) – listeria contamination (2023)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 8, 2023CA, CO, CT +17 more• Real Kosher Ice Cream, Inc.

Butter Flavored Popcorn (Bickel's) – Undeclared milk (2023)

Undeclared Milk

Undeclared milk

Class II

1...180 181182183 184...1066

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Moderate

FDAAug 8, 2023Nationwide• Bickel's Snack Foods Inc

Soft Serve Vanilla Chocolate (Real Kosher) – Listeria risk (2023)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 8, 2023CA, CO, CT +17 more• Real Kosher Ice Cream, Inc.

Soft Serve Caramel Vanilla (Real Kosher) – Listeria risk (2023)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 8, 2023CA, CO, CT +17 more• Real Kosher Ice Cream, Inc.

ADVIA Chemistry Iron Reagents (Siemens) – QC Result Bias (2023)

There is a potential for a positive bias on Quality Control (QC) and patient sample results when using some IRON_2 reagent wedge pairs. When the issue occurs, the observed bias will vary wedge to wedge.

Moderate

FDAAug 8, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Soft Serve Razzle n' Dazzle (Real Kosher) – Listeria risk (2023)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 8, 2023CA, CO, CT +17 more• Real Kosher Ice Cream, Inc.

Soft Zero Lite Peanut Butter (Real Kosher) – Listeria risk (2023)

Listeria

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 8, 2023CA, CO, CT +17 more• Real Kosher Ice Cream, Inc.

B. Braun NORM-JECT Luer Solo (B. Braun) – Packaging Sterility (2023)

The sterile blister packaging may be damaged, and sterility may be compromised

Low

FDAAug 7, 2023Nationwide• B. Braun Medical, Inc.

Pluvicto (Advanced Accelerator) – Incorrect Labeling (2023)

Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date

Class IIILow

FDAAug 7, 2023Nationwide• Advanced Accelerator Applications USA, Inc.

B. Braun NORM-JECT Luer Lock (B. Braun) – Packaging Sterility (2023)

The sterile blister packaging may be damaged, and sterility may be compromised

Low

FDAAug 7, 2023Nationwide• B. Braun Medical, Inc.

VITROS XT ALKP Slides (Ortho-Clinical) – Substrate Depletion (2023)

Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate deleption (DP) code, which may result in the System reporting an incorrect value (lower than the actual value), which may result in missed or delayed diagnosis of liver disease.

Moderate

FDAAug 5, 2023Nationwide• Ortho-Clinical Diagnostics, INc.

VITROS XT TBIL-ALKP Slides (Ortho-Clinical) – Substrate Depletion (2023)

Moderate

FDAAug 5, 2023Nationwide• Ortho-Clinical Diagnostics, INc.

EU7000is Portable Generators (Honda) – Fire risk (2023)

Fire/Burn Risk

This recall involves Honda Portable Generators with model number EU7000is. They are red and gray in color and measure about 33 inches long, 28 inches wide and 28 inches high. Honda and EU7000is are printed on the side of the generator. The following serial numbers are included in this recall: EEJD-1364963 through EEJD-1366026. The serial number decal is located inside the access door.

High

CPSCAug 3, 2023Nationwide• American Honda Motor Co. Inc., of Torrance, California

3T Heater Cooler System (LivaNova) – maintenance schedule error (2023)

The firm's labeling (Quick Reference Guide) contains incorrect information in the maintenance schedule for the Heater-Cooler device.

Low

FDAAug 3, 2023Nationwide• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

Sodium Chloride Injection (B. Braun) – Incomplete Labeling (2023)

Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.

Class IIILow

FDAAug 2, 2023Nationwide• B. Braun Medical Inc.

COOLIEF RF Generator (Avanos) – equipment fault increase (2023)

Avanos has received an increase in complaints from customers for COOLIEF RF Generators producing F100 and F101 faults.

Moderate

FDAAug 1, 2023AZ, CA, GA +13 more• Avanos Medical, Inc.

Magnifuse Bone Graft (Medtronic) – incorrect product labeling (2023)

The incorrect product labeling was applied to the product indicating the wrong size of product.

Moderate

FDAJul 31, 2023Nationwide• Medtronic Sofamor Danek USA Inc

Perifix Epidural Set (B. Braun) – mislabeled lid (2023)

Product may be mislabeled with an incorrect lid stock label.

Low

FDAJul 31, 2023AZ, AR, CA +10 more• B. Braun Medical, Inc.

Ford Transit (MIDWAY SPECIALTY) – fuel hose problem (2023)

Fire/Burn Risk

Midway Specialty Vehicles (Midway) is recalling certain 2022 Ford Transit vans equipped with certain Cummins Onan generators. The fuel hose between the inline fuel filter and the Injection Pump Module (IPM) may have inadequate clamp force, possibly resulting in a gasoline leak.

High

NHTSAJul 28, 2023Nationwide• MIDWAY SPECIALTY VEHICLES