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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

422

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 2001–2020 of 4598 recalls

GE Healthcare, LLC: Achilles Insight Bone Sonometer

Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.

FDASep 3, 2019Nationwide• GE Healthcare, LLC

GE Healthcare, LLC: Achilles Express Bone Sonometer

Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.

FDASep 3, 2019Nationwide• GE Healthcare, LLC

Apetina Marinated Olives & Feta (UNFI) – Temperature Mishandling (2019)

Product was held room temperature and the label stated to keep the product refrigerated.

Class IIModerate

1...99 100101102 103...230

Page 101 of 230Next

FDA

Sep 1, 2019

FL, IL, IN +4 more

• UNFI General Corporate

GE Healthcare, LLC: ApexPro Telemetry Server System. Also identified as Modi...

May not provide visual and/or audible alarms at the CARESCAPE Central Station or Clinical Information Center monitor for ECG arrhythmias, ECG LEADS FAIL or Pulse Oximetry (SpO2) under certain conditions.

FDAAug 30, 2019Nationwide• GE Healthcare, LLC

Pajunk GmbH Karl-hall-str. 1 Geisingen Germany: SPROTTE Lumbar with Introducer, labeled as the following:...

Problem with packaging sealing process which affects sterility.

FDAAug 30, 2019Nationwide• Pajunk GmbH Karl-hall-str. 1 Geisingen Germany

NxStage Medical, Inc.: Low Volume Cartridge IFU (SKU CAR-125-B) used with the fo...

There is a potential patient health risk while performing chronic hemodialysis treatments in the home setting with for patients with low blood volume (2.4 Liters or less in a patient with body weight of 30kg or less) when prescribing larger dialysate volumes.

FDAAug 27, 2019AL, AZ, CA +2 more• NxStage Medical, Inc.

LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany: Control Panel REF - 60-02-15: LivaNova SCP Pump Control ...

The SCP control Panel rotary knob used to control rotary speed of the pump in the SCP system used as a centrifugal pump during cardiopulmonary bypass may be difficult or impossible to rotate as a result of premature wear of the angle encoder. The loss of function of the angle encoder during bypass may lead to ischemia, stroke, organ damage, arterial tissue injury or reperfusion syndrome.

FDAAug 26, 2019FL, GA, IN +10 more• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany: Control Panel REF - 60-02-50: LivaNova SCP Pump Control ...

FDAAug 26, 2019FL, GA, IN +10 more• LivaNova Deutschland GmbH Lindberghstr. 25 Munich Germany

GETINGE US SALES LLC: The HEMASHIELD PLATINUM Woven Double Velour Vascular Graf...

Based on an internal incident report, Getinge/Intervascular SAS has identified that the one (1) HEMASHIELD GOLD Knitted Microvel Double Velour Vascular Bifurcated Graft product with the diameter size of 16 x 9 mm is likely incorrectly packed inside of the carton which was labeled to contain a HEMASHIELD PLATINUM Woven Double Velour Vascular Graft product with the diameter size of 16 x 8 mm ((REF: M00202166168P0, Lot: 18K31, SN: 1190443415, size 16 x 8 mm).

FDAAug 22, 2019NJ• GETINGE US SALES LLC

2019 VOLKSWAGEN BEETLE Recall: ELECTRICAL SYSTEM:IGNITION:ANTI-THEFT:CONTROL MODULE

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2015-2019 GTI, 2015-2016 and 2018-2019 Golf, 2012-2019 Beetle and Beetle Convertible, 2017-2019 Golf SportWagen and 2011-2018 Jetta vehicles equipped with an automatic transmission, manual handbrake and keyless entry. A build-up of silicate on the shift lever micro switch contacts may enable the key to be removed from the ignition when the transmission shift lever is not in "Park."

NHTSAAug 22, 2019Nationwide• VOLKSWAGEN

2019 VOLKSWAGEN ATLAS Recall: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY

Fire/Burn Risk

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Atlas vehicles. The suction jet in the fuel tank may have been welded in the incorrect position allowing fuel to leak. Additionally, the vehicle may stall due to uneven fuel distribution.

NHTSAAug 21, 2019Nationwide• VOLKSWAGEN

Golf Vehicles (Club Car) – Fire and Burn Risk (2019)

Fire/Burn Risk

This recall involves model year 2019 gas-powered Precedent, Tempo, Onward and Villager golf and transport vehicles, which are used for short-distance transportation. Vehicles with the following model and serial numbers are included in the recall. Serial numbers are located above and to the right of the accelerator pedal. The model number is the first two letters of the serial number. Model Name Model Number Serial Number Tempo Gas BX BX1905-944274 to BX2003-039920 Tempo Gas 2 + 2 BY BY1910-953754 to BY2002-039481 Onward 2 Pass Non-Lifted Gas BQ BQ1924-981193 to BQ2003-041072 Onward 4 Pass Non-Lifted BS BS1910-953760 to BS2003-041012 Onward 4 Pass Lifted Gas BW BW1910-953767 to BW2003-041068 Precedent Villager 2 Gas BJ BJ1910-953915 to BJ2002-039525 Precedent Gas EFI 2P DF DF1929-987941 to DF2002-039479 Precedent Villager 4 Gas DJ DJ1929-987934 to DJ1950-034968 Onward 6 Pass Non-Lifted Gas AY AY1945-024474 to AY1949-033252 Onward 6 Pass Lifted Gas AW AW1945-024474 to AW2003-041004

CPSCAug 19, 2019Nationwide• Club Car, of Augusta, Georgia

Normand-Info S.A.S.U. 7 rue Frederic Degeorge Arras CEDEX France: Remisol Advance running on hardware with Windows XP, Wind...

Laceration Risk

A patch was released for a critical remote code execution vulnerability in remote desktop services. This vulnerability can be exploited remotely without authentication on certain operating systems. An attacker who successfully exploited this vulnerability could execute arbitrary code on the target system; then install programs; view, change, or delete data; or create new accounts with full user rights. If the vulnerability could be exploited locally, it would lock down the computer.

FDAAug 15, 2019AL, AK, AZ +48 more• Normand-Info S.A.S.U. 7 rue Frederic Degeorge Arras CEDEX France

WOM World of Medicine AG Salzufer 8 Berlin Germany: Aquilex Fluid Control System component: Bag deflector, RE...

The deficit displayed by the pump can differ from the real deficit, leading potentially to patient risk.

FDAAug 14, 2019Nationwide• WOM World of Medicine AG Salzufer 8 Berlin Germany

GE Healthcare, LLC: Proteus XR/a (SlOK : K993090)

Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.

FDAAug 9, 2019Nationwide• GE Healthcare, LLC

Soothing Sore Relief Gel (Ridge Properties) – Superpotent Drug (2019)

Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.

Class IIModerate

FDAAug 9, 2019Nationwide• Ridge Properties, LLC

Soothing Sore Relief Cream (Ridge Properties) – Superpotent Drug (2019)

Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.

Class IIModerate

FDAAug 9, 2019Nationwide• Ridge Properties, LLC

Superior Pain Relief Cream (Ridge Properties) – Superpotent Drug (2019)

Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.

Class IIModerate

FDAAug 9, 2019Nationwide• Ridge Properties, LLC

Pre-Tat Lidocaine Gel (Ridge Properties) – Microbial Contamination (2019)

Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.

Class IIModerate

FDAAug 9, 2019Nationwide• Ridge Properties, LLC

Pre-Tat Lidocaine Cream (Ridge Properties) – Microbial Contamination (2019)

Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.

Class IIModerate

FDAAug 9, 2019Nationwide• Ridge Properties, LLC