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Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

Radiometer Medical ApS Akandevej 21 Bronshoj Denmark Recalls

All product recalls associated with Radiometer Medical ApS Akandevej 21 Bronshoj Denmark.

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Recall Summary

Total Recalls

1000

Past Year

432

Class I (Serious)

138

Most Recent

Dec 2025

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 3201–3220 of 7663 recalls

ABL90 FLEX Analyzer (Radiometer) – barcode reader error (2020)

The firm received reports of occurrences where the barcode reader misinterpreted the contents of a locally printed barcode label used for entering patient ID or accession number into the analyzer in connection with a sample measurement. This could result is patient mixup and/or lost of sample, resulting in delayed medical treatment.

FDAFeb 3, 2020Nationwide• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

TRUMATCH Orthognathic Kit (Materialise) – incorrect plate labeling (2020)

Custom surgical kits contain a plate different than indicated by the package labeling.

FDAFeb 3, 2020NY• Materialise N.V. Technologielaan 15 Heverlee Belgium

Rompe Pecho EX (Efficient Labs) – Microbial Contamination (2020)

Microbial Contamination of Non-Sterile Products

Class II

1...159 160161162 163...384

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Moderate

FDAJan 31, 2020Nationwide• Efficient Laboratories, Inc.

Rompe Pecho MAX (Efficient Labs) – Microbial Contamination (2020)

Microbial Contamination of Non-Sterile Products

Class IIModerate

FDAJan 31, 2020Nationwide• Efficient Laboratories, Inc.

Rompe Pecho CF (Efficient Labs) – Microbial Contamination (2020)

Microbial Contamination of Non-Sterile Products

Class IIModerate

FDAJan 31, 2020Nationwide• Efficient Laboratories, Inc.

Mercedes-Benz A 220 (Mercedes-Benz) – rearview camera software (2020)

Mercedes-Benz USA, LLC. (MBUSA) is recalling certain 2019 A220 and A220 4MATIC vehicles. In certain operating conditions, the rearview camera software may cause a delay in displaying the rearview camera image. As such, these vehicles fail to comply to Federal Motor Safety Standard (FMVSS) number 111, "Rearview Mirrors."

NHTSAJan 28, 2020Nationwide• MERCEDES-BENZ

Mercedes-Benz AMG GT63 (Mercedes-Benz) - Transmission Wiring Issue (2020)

Mercedes-Benz USA, LLC. (MBUSA) is recalling certain 2019 AMG GT63 4MATIC and AMG GT63S 4MATIC vehicles. A wiring harness for the automatic transmission may not be properly secured, allowing it to chafe against the drive shaft and possibly cause an engine stall.

NHTSAJan 28, 2020Nationwide• MERCEDES-BENZ

Mercedes-Benz AMG GT63 (Mercedes-Benz) - Engine Cooling Concern (2020)

Fire/Burn Risk

Mercedes-Benz USA, LLC. (MBUSA) is recalling certain 2018-2019 E63 AMG 4MATIC, E63S AMG 4MATIC Wagon, S63 AMG Cabrio 4MATIC, S63 AMG Coupe 4MATIC, and S63 AMG 4MATIC and 2019 G63 AMG 4MATIC, AMG GT63 4MATIC, AMG GT63S 4MATIC vehicles equipped with 4.0L 8-cylinder gasoline turbocharged engines. The oil feed line to the turbocharger may leak.

NHTSAJan 27, 2020Nationwide• MERCEDES-BENZ

Olmesartan Tablets (Ascend) – API Source Deviation (2020)

cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.

Class IIModerate

FDAJan 24, 2020Nationwide• Ascend Laboratories LLC

LN 3R70-01 Software (Abbott) - Performance Potential Issues (2020)

Abbott has identified potential performance issues for the Alinity ci -series Software version 2.6.2 and earlier.

FDAJan 24, 2020Nationwide• Abbott Gmbh & Co. KG Max-Planck-Ring 2 65205 Wiesbaden Germany

Minocycline Hydrochloride Tablets (Ascend) – Failed Dissolution (2020)

Failed Dissolution Specifications: low out of specification results for dissolution testing.

Class IIILow

FDAJan 22, 2020Nationwide• Ascend Laboratories LLC

FlipCutter III Drill (T.A.G. Medical) - Sterile Barrier Compromise (2020)

There is potential for the blister tray to be cracked causing the sterile barrier to be compromised and potential for particulate within the sterile barrier.

FDAJan 20, 2020Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton Naharia Israel

Ground Ginger (H.L. Foodservice) – Sulfite Labeling Issue (2020)

Ground ginger does not properly identify addition of sulfites on the package label.

Class IIModerate

FDAJan 17, 2020CA• H.L. Foodservice, Inc. dba H.L. Foods Co.

SnapLink L6R (Ormco) - Buccal Tube Door Malfunction (2020)

The action is being taken due to an increase in complaints relating to the lower buccal tube slide doors not staying close. In the event of functional failure, broken/damage buccal tubes it may cause the tooth to rotate, possibly delay treatment and inconvenience the patient and clinician. If not noticed it may extend treatment by approximately 1 -3 months.

FDAJan 17, 2020AL, AK, AZ +48 more• Ormco/Sybronendo