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Genesis Partnership Company SA

Genesis Partnership Company SA Recalls

All product recalls associated with Genesis Partnership Company SA.

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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 1741–1760 of 4598 recalls

Panagel Hand Sanitizer (Genesis Partnership) – Manufacturing Deviation (2020)

CGMP Deviations: hand sanitizers were recalled because they were manufactured in the same facility as another hand sanitizer product with sub-potent ethanol levels.

Class IIModerate

FDASep 11, 2020Nationwide• Genesis Partnership Company SA

2020 GENIE TZ-50 Recall: STRUCTURE

Genie Industries, Inc. (Genie) is recalling certain 2020 TZ-50 trailers. The bolted joints of the tongue structure may loosen and possibly separate from the main chassis.

NHTSASep 10, 2020Nationwide• GENIE

GE Healthcare, LLC: System, Nuclear Magnetic Resonance Imaging - Product Usag...

Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

FDA

1...86 878889 90...230

Page 88 of 230Next

Sep 8, 2020

Nationwide

• GE Healthcare, LLC

GE Healthcare, LLC: Tomographic Imager Combining Emission Computed Tomography...

Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.

FDASep 8, 2020Nationwide• GE Healthcare, LLC

CO2 Canisters (Soda Sense) - Injury Hazard (2020)

This recall involves type 2 SODA SENSE 0.6 liter CO2 canisters sold through the SODA SENSE mail order exchange program. The metal, cylinder canisters are silver with a black cap. The SODA SENSE logo appears on the front of each canister. Only those cylinders with two (2) indented rings on the bottom are the subject of this recall.

CPSCSep 3, 2020Nationwide• CO2 Exchange LLC, dba SODA SENSE, of Green Bay, Wis.

2020 VOLKSWAGEN PASSAT Recall: AIR BAGS:PASSENGER SIDE FRONTAL:CUSHION

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2020 Passat vehicles. The passenger frontal air bag may have been folded incorrectly affecting its deployment force. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection."

NHTSASep 2, 2020Nationwide• VOLKSWAGEN

Gentian AS Bjornasveien: GENTIAN Cystatin C Calibrator and Calibrator Kit, for the...

The firm has identified lots of calibrators that have shown to measure incorrect high values over time compared to the assigned values when released for distribution. This could result in higher Cystatin C values measured in patients.

FDASep 2, 2020KS, MN, VA• Gentian AS Bjornasveien

Brainlab AG Olof-palme-str. 9 Munich Germany: Ultrasound Navigation Software 1.0 and Ultrasound Integra...

Brainlab Ultrasound Navigation Software does not support the modification of the probe's image width.

FDAAug 31, 2020Nationwide• Brainlab AG Olof-palme-str. 9 Munich Germany

2018 DODGE CHARGER Recall: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

Chrysler (FCA US LLC) is recalling certain 2018-2020 Dodge Charger Pursuit vehicles equipped with a "stealth mode." When stealth mode is selected, the backup camera rearview image will not display when the vehicle is in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rearview Mirrors."

NHTSAAug 27, 2020Nationwide• DODGE

2020 VOLKSWAGEN ATLAS CROSS SPORT Recall: EXTERIOR LIGHTING:HEADLIGHTS

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2020 Atlas Cross Sports and 2021 Atlas vehicles. The driver's side headlight may have been aimed too low during production. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSAAug 26, 2020Nationwide• VOLKSWAGEN

Genicon, Inc.: Aquas PowerFlow Tube Set - Product Usage: The device deli...

The product design incorporating a motor driven impeller pump powered by one 9V alkaline battery inside the hand-piece did not receive proper premarket clearance from US FDA and lacks a 510(k).

FDAAug 25, 2020Nationwide• Genicon, Inc.