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Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany

Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany Recalls

All product recalls associated with Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany.

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Recall Summary

Total Recalls

1000

Past Year

726

Class I (Serious)

175

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 11124 recalls

DxA 5000 (Beckman Coulter) – Sample ID Confusion (2020)

The DxA 5000 instructions for use may be confusing regarding the re-use of sample IDs. Beckman Coulter has received complaints where the re-use of sample barcodes were not being detected by the system .

Low

FDAJun 17, 2020Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munich Germany

Jetta (Volkswagen) – Brake Caliper Bolt Risk (2020)

Volkswagen Group of America, Inc. (Volkswagen) is recalling one 2020 Jetta vehicle. The front brake caliper bolts may come loose.

High

NHTSAJun 17, 2020Nationwide• VOLKSWAGEN

MatrixMIDFACE Screws (Synthes) – Incorrect Screw Packaging (2020)

One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).

Low

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FDAJun 16, 2020IN• Synthes Produktions GmbH Eimattstrasse

Childrens Dimetapp Cold & Cough (Glaxosmithkline) – Defective Dosing Cup (2020)

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Class IIModerate

FDAJun 16, 2020Nationwide• Glaxosmithkline Consumer Healthcare Holdings

Childrens Robitussin Honey Cough (Glaxosmithkline) – Defective Dosing Cup (2020)

Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.

Class IIModerate

FDAJun 16, 2020Nationwide• Glaxosmithkline Consumer Healthcare Holdings

Raptor (Keystone) – Window Glass Adhesive Failure (2020)

Keystone RV Company (Keystone) is recalling certain 2020 Alpine, Avalanche, Fuzion, Laredo, Montana, Raptor, Crossroads Redwood, and Dutchmen Voltage trailers. The adhesive bond between the glass and the metal frame of the frameless windows may fail which can allow the glass to detach while moving.

High

NHTSAJun 12, 2020Nationwide• KEYSTONE

Prestige (Lode King) – Incorrect Load Rating Decal (2020)

Lode-King Industries LTD. (Lode-King) is recalling one 2021 Prestige SDG semi-trailer. The incorrect load rating decal has been applied, showing a load rating for the trailer frame that exceeds its strength capability.

High

NHTSAJun 11, 2020Nationwide• LODE KING

Irinotecan Injection (Hikma Pharmaceuticals) – Crimp Defect (2020)

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Class IIModerate

FDAJun 11, 2020Nationwide• Hikma Pharmaceuticals USA Inc.

Irinotecan Injection (Hikma Pharmaceuticals) – Crimp Defect (2020)

Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use.

Class IIModerate

FDAJun 11, 2020Nationwide• Hikma Pharmaceuticals USA Inc.

Leksell Vantage System (Elekta) – Locking Mechanism Failure (2020)

The locking mechanism at the interface of the Instrument Carrier and the Leksell Vantage Arc may not function properly.

Low

FDAJun 10, 2020AZ, FL, IL +11 more• Elekta Instrument AB Kungstensgatan 18 Stockholm Sweden

Nabumetone Tablets (American Health Packaging) – Incomplete Labeling (2020)

Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with the accompanying Medication Guide was not included on the carton label.

Class IIILow

FDAJun 10, 2020Nationwide• American Health Packaging

Accurian RF Ablation Cannula (Medtronic) – Probe Insertion Issue (2020)

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Low

FDAJun 8, 2020Nationwide• Medtronic Sofamor Danek USA Inc

Lokomat Pro (Hocoma) – Motor Controller Failure (2020)

The motor controller may fail, which can potentially lead to an error in functionality of the Body Weights Support Rope, which means that the rope can go up or down in an uncontrolled way.

High

FDAJun 8, 2020Nationwide• Hocoma AG Industriestrasse 4 Volketswil Switzerland