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Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany

Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany Recalls

All product recalls associated with Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany.

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Recall Summary

Total Recalls

1000

Past Year

899

Class I (Serious)

125

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 341–360 of 17592 recalls

Fortress Introducer Sheath (Contract Medical) – labeling error (2025)

Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version.

Low

FDAJul 30, 2025Nationwide• Contract Medical International GmbH Lauensteiner Str. 37 Dresden Germany

10Fore Hemostasis Valve (Merit Medical) – Silicone Ring Defect (2025)

Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.

Moderate

FDAJul 25, 2025Nationwide• Merit Medical Systems, Inc.

Electrosurgical Generator (Olympus) – system error (2025)

Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot 'loops'.

1...16 171819 20...880

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Moderate

FDAJul 25, 2025Nationwide• Olympus Corporation of the Americas

ZAP-X Radiosurgery System (Zap Surgical) – proximity error (2025)

If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after the automatic reduction of speed, a software defect could potentially lead the collimator to collide with patient shoulders or the patient table.

High

FDAJul 25, 2025Nationwide• Zap Surgical Systems

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAJul 25, 2025AZ, IN, NJ• Breckenridge Pharmaceutical, Inc.

Doxepin Hydrochloride Capsules (Alembic) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.

Class IIModerate

FDAJul 25, 2025Nationwide• Alembic Pharmaceuticals Limited

Frigidaire Minifridges (Curtis International) – fire hazard (2025)

Fire/Burn Risk

This recall involves Curtis International minifridges. "Frigidaire" is printed on the front of the units. The model and serial numbers are on a label on the back of the minifridge. The model numbers of the affected units are: EFMIS129, EFMIS137, EFMIS149 and EFMIS175. The minifridges were sold in 6- and 9-Can sizes. Recalled minifridges include only the serial numbers identified below. The minifridges were sold in a variety of colors, including black, blue, green, white, yellow, red, pink and silver. Model Number Serial Number EFMIS129 Between A2001 to A2308 - if model number is "EFMIS129-B" or EFMIS129-C", it is not included in this recall. EFMIS137 Between A2001 to A2312 EFMIS149 Between A2001 to A2308 EFMIS175 Between A2001 to A2310

High

CPSCJul 24, 2025Nationwide• ShangYu North Electron Manufacture Co. Ltd., of China

Dexcom G7 CGM System (Dexcom) – Software Compatibility Issue (2025)

The affected devices are the Dexcom G7 Continuous Glucose Monitoring System (CGM System) using iOS, watchOS and Android App software (versions 2.8.0 or earlier) and Dexcom ONE+ CGM System using iOS and Android App software (versions 1.4.0 or earlier), henceforth referred to as the App. The affected App does not provide an expected "Sensor Failed" alert when the transmitter sends a "transmitterFailed" error message to the App when the CGM experiences a hardware or firmware failure. Instead, the App ends the CGM sensor session, stops reporting glucose values and displays the Start Sensor screen or No active sensor message without alerting the user, which can lead to missed detection of a hyperglycemic or hypoglycemic event and a delay in treatment.

High

FDAJul 24, 2025Nationwide• Dexcom, Inc.

Dexcom ONE+ CGM System (Dexcom) – Software Compatibility Issue (2025)

High

FDAJul 24, 2025Nationwide• Dexcom, Inc.

Park Street Deli Cinnamon Bun Dip (Superior Foods) – foreign material (2025)

foreign material (plastic)

Class IIModerate

FDAJul 24, 2025Nationwide• Superior Foods Company

Cheddar Bagel (Bonami Baking) – undeclared wheat milk (2025)

Undeclared Gluten

Undeclared wheat and milk from sub-ingredients.

Class IIModerate

FDAJul 24, 2025CA• The Bonami Baking Company, Inc.

Whole Grain Jalapeno Bagel (Bonami Baking) – undeclared milk (2025)

Undeclared Milk

Undeclared milk from Contains statement.

Class IIModerate

FDAJul 24, 2025CA• The Bonami Baking Company, Inc.

Chocolate Croissants (Bonami Baking) – undeclared wheat milk (2025)

Undeclared Gluten

Undeclared wheat, milk, and soy (from soy lecithin) from sub-ingredients.

Class IIModerate

FDAJul 24, 2025CA• The Bonami Baking Company, Inc.

Wheat Hamburger Buns (Bonami Baking) – Undeclared Allergens (2025)

Undeclared Milk

Undeclared milk and/or eggs from sub-ingredients and/or Contains statement.

Class IIModerate

FDAJul 24, 2025CA• The Bonami Baking Company, Inc.

Whole Wheat Chocolate Croissants (Bonami Baking) – undeclared milk soy (2025)

Undeclared Milk

Undeclared milk and soy (from soy lecithin) from sub-ingredients.

Class IIModerate

FDAJul 24, 2025CA• The Bonami Baking Company, Inc.

NovoTHOR (Thor) – Gas Strut Welding Failure (2025)

The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.

Moderate

FDAJul 24, 2025Nationwide• THOR Photomedicine Ltd 2 Anglo Office Park Units 1 &; 67 White Lion Road Amersham United Kingdom