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GE Medical Systems, LLC

GE Medical Systems, LLC Recalls

All product recalls associated with GE Medical Systems, LLC.

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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 4881–4900 of 21320 recalls

Centricity Universal Viewer (GE Medical) – Hidden Studies (2022)

There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in reading the study.

Moderate

FDAOct 28, 2022Nationwide• GE Medical Systems, LLC

Centricity PACS-IW (GE Medical) – Hidden Studies (2022)

Moderate

FDAOct 28, 2022Nationwide• GE Medical Systems, LLC

Evolution MP Tibial Bases (MicroPort) – Incorrect Component (2022)

One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.

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Low

FDAOct 28, 2022Nationwide• MicroPort Orthopedics Inc.

Micro Bird G5 Transit Bus (Micro Bird) – Power Steering Line (2022)

Corp. Micro Bird Inc. (Micro Bird) is recalling one 2019 Micro Bird G5 transit bus. An inadequate connection between the power steering pressure line and the brake Hydroboost unit may result in a sudden loss of power steering fluid.

Moderate

NHTSAOct 28, 2022Nationwide• MICRO BIRD

Kalera Krunch Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

Kalera Butter Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

Kalera Baby Romaine Lettuce - salmonella risk (2022)

Salmonella

Potential contamination with Salmonella

Class IHigh

FDAOct 28, 2022Nationwide• Kalera Public Limited Company

Micro Bird G5 School Bus (Micro Bird) – Power Steering (2022)

Corp. Micro Bird Inc. (Micro Bird) is recalling certain 2019-2022 Micro Bird G5 school buses. An inadequate connection between the power steering pressure line and the brake Hydroboost unit may result in a sudden loss of power steering fluid.

Moderate

NHTSAOct 28, 2022Nationwide• MICRO BIRD

Southmedic Safety Cartridge (Southmedic) – Sterilization Issue (2022)

Upon review of its batch record, Southmedic identified that lot # W92761 was not sent out for sterilization, and was instead transferred directly to distribution where it was sold and distributed to customers as non-sterile product labelled as sterile.

Moderate

FDAOct 27, 2022Nationwide• Southmedic, Inc.

Tesla Cyberquad (Radio Flyer) – safety violation (2022)

This recall involves all Tesla Cyberquad for Kids by Radio Flyer, Model Number 914. The Cyberquad features a full steel frame, cushioned seat and adjustable suspension with rear disk braking and LED light bars. The Cyberquad is powered by a lithium-ion battery with up to 15 miles of range and a top speed of 10 mph. The Cyberquad has both the Tesla "T" and Radio Flyer logos printed on the battery. Information embossed into the underside of the seat identifies the product as Radio Flyer Model 914.

Moderate

CPSCOct 27, 2022Nationwide• Feishen Vehicle Industry Co LTD, of China

Immulite Testosterone Assay (Siemens) – Positive Bias (2022)

Confirmed an average positive bias of 40% for testosterone concentrations of approximately 660 ng/dL (22.9 nmol/L) and above with the IMMULITE/IMMULITE 1000 Total Testosterone Assay when compared to the IMMULITE 2000/IMMULITE 2000 XPi Total Testosterone Assay. Two (2) lots of Total Testosterone assays for the IMMULITE/IMMULITE 1000, kit lots #515 and #516 were actively distributed to customers when the issue was discovered by Siemens, and they are subject to the correction or removal in this recall (867 total quantity of reagents distributed for each lot). The violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. In both males and female, testosterone results are not used in isolation but are interpreted in conjunction with clinical history and symptomology as well as with other laboratory testing (e.g. gonadotropins and other sex steroids). A delay in the diagnosis may be experienced and medical intervention, such as repeat testing may be required.

Moderate

FDAOct 25, 2022Nationwide• Siemens Healthcare Diagnostics, Inc.

eSuction Small Cavity (Endo-Therapeutics) – Regulatory Issue (2022)

Improper device regulatory classification

Moderate

FDAOct 24, 2022FL, PA• Endo-Therapeutics, Inc.

Philips ProxiDiagnost N90 (Philips) – Tabletop Cable (2022)

Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking

Moderate

FDAOct 21, 2022Nationwide• Philips North America Llc

Simplex HV Bone Cement (Howmedica) – Distribution Error (2022)

Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to customers who had ordered Simplex HV With Gentamicin in US, 10 PACKS (P/N 6195-1-010)

Moderate

FDAOct 21, 2022Nationwide• Howmedica Osteonics Corp.

NEO-fit Endotracheal Grip (CooperSurgical) – Clip Detachment (2022)

Laceration Risk

Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was removed from the patient's mouth. In one case, the patient suffered a laceration to the throat.

High

FDAOct 20, 2022Nationwide• CooperSurgical, Inc.

Carrier Transicold Unit (Carrier) – Electrical Issue (2022)

Fire/Burn Risk

Carrier Corporation (Carrier) is recalling certain Carrier Transicold Refrigeration Units, model NDTP Supra S Series (S6, S7, S8, S9, S10). The 12-Volt wire harness on the truck refrigeration unit (TRU) may be exposed and missing heat shrink, which can cause electrical arcing.

High

NHTSAOct 20, 2022Nationwide• CARRIER TRANSICOLD

Atrium Ocean Chest Drain (Atrium) – Temperature Excursion (2022)

Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.

Low

FDAOct 18, 2022Nationwide• Atrium Medical Corporation

Buprenorphine and Naloxone Sublingual Tablets (Sun Pharmaceutical) – Foreign Substance (2022)

Presence of Foreign Substance

Class IIModerate

FDAOct 18, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Accelerate PhenoTest BC Kit (Accelerate) – False Positive Risk (2022)

Due improperly formulated and released bulk lot of fluorescence in situ hybridization (FISH) probes resulting in false positive identification results for Staphylococcus aureus and Streptococcus spp.

Moderate

FDAOct 17, 2022AR, CA, FL +28 more• Accelerate Diagnostics Inc

Visualase Cooled Laser Applicator (Medtronic) – Sterile Seal Defect (2022)

Due to a defect in the outer pouch sterile seal

Moderate

FDAOct 14, 2022Nationwide• Medtronic Navigation, Inc.