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Siemens Healthcare Diagnostics, Inc.

Siemens Healthcare Diagnostics, Inc. Recalls

All product recalls associated with Siemens Healthcare Diagnostics, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 34021–34040 of 37665 recalls

Siemens Healthcare Diagnostics, Inc.: Dimension Flex Reagent Cartridge Cardiac Tropinin-I, Cata...

Tests exhibit falsely elevated results.

FDAMar 2, 2007Nationwide• Siemens Healthcare Diagnostics, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator. The device is a battery o...

LIFEPAK CR Plus defibrillators with software version 1.16 or lower may miscalculate the HLC battery capacity and result in the CHARGE-PAK battery charger icon/indicator to display and falsely indicate battery needs replacement.

FDAMar 2, 2007IN, OR• Medtronic Emergency Response Systems, Inc.

Teleflex Medical: Conditional Fiber Optic Laryngoscope Kit, which contains ...

The MRI Battery is out of specification for its magnetic content.

1...1700 170117021703 1704...1884

Page 1702 of 1884Next

GA

• Teleflex Medical

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Suture Passer 2 inch Part Number : 7209167

Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.

FDAMar 1, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

GE OEC Medical Systems, Inc: OEC 9900 Elite (NAV) Image-intensified fluoroscopic x-ray...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 8800 image-intensified fluoroscopic x-ray system, GE ...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

Philips Medical Systems (Cleveland) Inc: Philips, Voxel Q workstations, untilizing AcQSim or AcQP...

Incorrect simulation and/or beam placement: An anomaly has been identified with the Philips VoxelQ workstation utlizing AcQPlan software version 4.2, 4.2.1, 4.9, 4.9.1, 4.9.2, 4.9.3, 5.0, 5.0.1, 5.0.2 or 5.0.3 when computing absolute patient marking coordinates with data containing reconstruction offsets from the Mx800, the Mx8001DT, and the Brilliance 6, 10, 16, 16P, and Big Bore CT systems. Whe

FDAMar 1, 2007AL, AZ, AR +43 more• Philips Medical Systems (Cleveland) Inc

GE OEC Medical Systems, Inc: OEC 9900 Elite MD Motorized C-Arm System, image-intensifi...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 MD Motorized C-Arm System, image-intensified flu...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Suture Passer 12 inch Part Number: 7209166

Product is labeled as reusable but there is a potential that the cannulated handle of the product cannot be cleaned adequately following use.

FDAMar 1, 2007Nationwide• Smith & Nephew, Inc. Endoscopy Division

GE OEC Medical Systems, Inc: OEC 9900 Elite image-intensified fluoroscopic x-ray syste...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic ...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 image-intensified fluoroscopic x-ray system, GE ...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus (Fluorotrak), Image-intensified fluoroscopi...

During routine service, primary and/or secondary collimators may not have been properly reinstalled.

FDAMar 1, 2007Nationwide• GE OEC Medical Systems, Inc

Mizuho Orthopedic Systems Inc: OSI ProFx Operating Room Table 6850 , Pelvic Reconstructi...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, Allegro 6800 Imaging Table (Operating), single pedes...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Mizuho Orthopedic Systems Inc: OSI, 6822 IntraOp Series Tables, Operating Room tables, O...

Failure to anchor; due to a failure in the locking mechanism, the product may not anchor properly.

FDAFeb 28, 2007AL, AZ, CA +28 more• Mizuho Orthopedic Systems Inc

Digital Dive Computers (Pelagic) – Decompression Risk (2007)

The recall involves Oceanic-brand ATOM 2.0 dive computers with serial numbers 1 through 2,079 (Revisions 2E, 3A, and 3B) and AERIS-brand EPIC dive computers with serial numbers 1 through 712 (Revision 1A), which can be accessed and viewed on the computer's display. Also, the serial number and date of manufacture are printed on the bottom of the unit (Oceanic ATOM 2.0 from August 23 to November 23, 2006, and AERIS EPIC from October 18 to November 14, 2006). This recall does not include any other Oceanic or AERIS brand dive computers.

CPSCFeb 28, 2007Nationwide• Pelagic Pressure Systems, of San Leandro, Calif.

Philips Medical Systems: Philips HeartStart FR2+ Defibrillator Automated External...

Failure of tactile switches on one of two printed circuit board assemblies (PCBA) used in the FR2+ device. Potential delay or prevention of shock treatment due to PCBA board contamination, causing intermittent switch operation.

FDAFeb 28, 2007Nationwide• Philips Medical Systems

Bio-Logic Systems Corp: Bio-logic-Ceegraph/Sleepscan Netlink Traveler, Bio-logic ...

Battery and Battery Compartment; incorrect placement in the Netlink Traveler unit which caused a short in the wiring of the battery pack and overheating.

FDAFeb 26, 2007Nationwide• Bio-Logic Systems Corp