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Btt Health Gmbh Billerberg 7 Inning Germany

Btt Health Gmbh Billerberg 7 Inning Germany Recalls

All product recalls associated with Btt Health Gmbh Billerberg 7 Inning Germany.

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Recall Summary

Total Recalls

624

Past Year

Class I (Serious)

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 81–100 of 624 recalls

Marodyne-LiV (BTT Health) – Power Supply Interruption (2024)

Some power supply units in Austria and Germany had a voltage drop in the millisecond range, which led to a cancellation of the treatment and subsequent restart of the medical device. The treatment is only restarted by a step-off/step-on (step-on for activation).

FDAAug 1, 2024Nationwide• Btt Health Gmbh Billerberg 7 Inning Germany

PE Centrifuge, REF: B36365, a component of the Power Express (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.

FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

Power Express, REF B90918 (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

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FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

PE Centrifuge Temperature Controlled, REF: B36366, a comp... (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

ARTIS Angiography System (Siemens) – Detector Potential Issue (2024)

A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.

FDAJun 26, 2024Nationwide• Siemens AG/Siemens Healthcare GmbH Rittigfeld 1 Forchheim Germany

CentriMag Primary Console (Thoratec) – Power Standard Nonconformance (2024)

Due to a component change, the console part of a circulatory support system may not conform to the IEC 61000-4-5 standard, so if subjected to a power surge above 1.8kV and up to 2.0 kV, the console may shut down completely without alarm, pumping would cease, and the patient would have to be switched to a backup circulatory support system.

FDAMay 22, 2024Nationwide• Thoratec Switzerland GMBH Technoparkstrasse 1 Zurich Switzerland

Endo Model M Tibial Components (Waldemar Link) – Surgical Screw Issue (2024)

Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

FDAMay 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Endo Model SL Tibial Components (Waldemar Link) – Surgical Screw Problem (2024)

Blind screws of the modular tibial component cannot be loosened intraoperatively,prolongation surgery due to intraoperatively change in procedure, probably to cementing technique

FDAMay 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

HistoCore Arcadia H (Leica) – Smoke and Fire Hazard (2024)

Fire/Burn Risk

An issue with safe usage of the device was identified whereby toxic smoke and internal fire developed resulting from a problem associated with the sealing of the paraffin tank.

FDAMay 10, 2024Nationwide• LEICA BIOSYSTEMS NUSSLOCH GMBH Heidelberger Str. 17-19 Nussloch Germany

Hoffman LRF Wire Tensioner (Stryker) – Adjustment Ring Issue (2024)

The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.

FDAMay 9, 2024Nationwide• Stryker GmbH Bohnackerweg 1 Selzach Switzerland

GMC Hummer EV Pickup (GMC) – Electrical System Issue (2024)

General Motors, LLC (GM) is recalling certain 2024 Cadillac Lyriq, Chevrolet Blazer EV, Chevrolet Silverado EV, GMC Hummer EV SUV, and GMC Sierra EV vehicles. The electric motors in the rear drive units may have insufficiently insulated wires that can contact each other, resulting in a loss of drive power.

NHTSAMay 9, 2024Nationwide• GMC

Vivid Ultrasound (GE Vingmed) – DICOM Worklist Issue (2024)

GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.

FDAMay 2, 2024IL, MA, NM +2 more• GE Vingmed Ultrasound As Strandpromenaden 45 Horten Norway

Commercial Refrigerators (Secop) – fire hazard (2024)

Fire/Burn Risk

This recall involves commercial refrigerators with Secop compressors with model number NLE11MN. The recalled Secop Compressors installed in True Commercial Refrigerators were sold through corporate channels to commercial customers and to the commercial food service companies. The recalled commercial refrigerators are both black and stainless steel in color, and have configurations with double, triple, and sliding doors. The model and serial numbers are printed on a label located inside the commercial refrigerator cabinet by the left door. The following refrigerator models and serial numbers are included in this recall: Refrigerator Model First serial number Last serial number GDIM-49NT 9466976 10040916 GDM-45 9344197 10010080 GDM-47 9300299 10010063 GDM-47FC 9344301 10010081 GDM-47RL 9342885 10049968 GDM-49 9301457 10009796 GDM-49FC 9343416 9994430 GDM-49RL 9347552 10049976 GDM-69 9302194 10049977 GDM-69FC 9368706 10042783 GDM-72 9303855 10048931 GDM-72FC 9346330 10048907 T-49G 9789525 9872836 TSD-47 9364752 10042789 TSD-47G 9342889 10049972

CPSCMay 2, 2024Nationwide• Secop GmbH, of Germany (compressors

Wegman's Half Loaf Garlic Bread (Wegmans Food Markets, Inc.) – undeclared milk (2024)

Undeclared Milk

Contains undeclared milk

Class IIModerate

FDAApr 25, 2024NY, PA• Wegmans Food Markets, Inc.

Mi1250 SYNCHRONY 2 (MED-EL) – internal electronics crack (2024)

A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.

FDAApr 18, 2024NC• MED-EL Elektromedizinische Gereate, Gmbh Furstenweg 77a Innsbruck Austria

Leica HistoCore PEGASUS Processor (Leica) – reagent level issue (2024)

Poorly processed and/or damaged biopsy tissue specimens on the device resulting from reagent levels exceeding the maximum fill level marks on reagent bottles or in the paraffin tanks.

FDAApr 10, 2024Nationwide• LEICA BIOSYSTEMS NUSSLOCH GMBH Heidelberger Str. 17-19 Nussloch Germany

Urinalysis Test Strips (Macherey Nagel) – Missing Test Pad (2024)

The reason for the recall is one of the test pads, for the parameter leukocytes, was missing on some of the test strips. The issue was identified by a consumer by way of a Henry Schein Inc. (HSI) customer complaint. This problem can potentially result in the possibility that the parameter leucocytes (a non-specific marker for urinary track infections and an indicator for inflammatory renal processes) is interpreted instrumentally as a false negative. The following HSI item number and lot number were affected: Urispec 11-Way, #102-2285, LOT 65402.

FDAApr 4, 2024Nationwide• Macherey Nagel Gmbh & Co. Kg Valencienner Str. 11 Duren Germany

Scopis ENT Software (Stryker) – Visual Feedback Misalignment (2024)

Unreleased software was installed on customer systems resulting in the visual feedback on the screen to show the points to be off from the physical reference point of the pointer or suction.

FDAApr 4, 2024Nationwide• Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany

Mainstays Electric Mini Choppers – Laceration Risk (2024)

Laceration Risk

This recall involves Mainstays Electric Mini Choppers with model number MS14100094536S1. The choppers are rechargeable and cordless, and have a green lid, white body, and clear plastic bowl. They have one blade attachment, which consists of three curved blades on one white plastic spindle. Model number MS14100094536S1 is on the label attached to the bottom of the clear plastic bowl.

CPSCApr 4, 2024Nationwide• Shuangma Plastic Manufacturing Inc., of China

Dynamic Mesh Implant (Stryker) – Mislabeling Issue (2024)

Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure

FDAMar 29, 2024Nationwide• Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany