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Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc. Recalls

All product recalls associated with Medtronic Emergency Response Systems, 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 33781–33800 of 37665 recalls

Medtronic Emergency Response Systems, Inc.: biphasic LIFEPAK 500 automated external defibrillators (A...

Reduced Shock- the device may deliver 100 Joule (J) to a patient, which is less than the recommended factory minimum default setting of 200 J.

FDAJun 13, 2007Nationwide• Medtronic Emergency Response Systems, Inc.

GE OEC Medical Systems, Inc: GE OEC 6800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 8800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007

1...1688 168916901691 1692...1884

Page 1690 of 1884Next

CO, FL, GA +4 more

• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoroscopic X-ray System, GE Healthcare, Sal...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 2800 mobile Fluoroscopic X-ray System, GE Healthca...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopic X-ray System, GE Healthcar...

X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.

FDAJun 12, 2007CO, FL, GA +4 more• GE OEC Medical Systems, Inc

Philips Medical Systems: Philips Medical HeartStartXL Defibrillator/Monitor Model ...

The ECG signal may become unusable to assess patient condition and need for therapy.

FDAJun 11, 2007Nationwide• Philips Medical Systems

Thoratec Corp: Thoratec TLC-II Portable VAD Driver. Component (pneumati...

Component Failure; Device Failure without warning; due to premature wear-out of the compressor motor, VAD support for the patient's circulatory system may fail without warning.

FDAJun 8, 2007AL, AZ, AR +25 more• Thoratec Corp

Thermador Ceramic Cooktops – fire hazard (2007)

Fire/Burn Risk

The cooktop has electric and induction heating elements with a black ceramic glass surface. This recall involves model numbers CIT302DS/01 and CIT362DS/01 with date codes between 8606 and 8612. The model number and date code can be found on the underside of the cooktop.

CPSCJun 7, 2007Nationwide• BSH Home Appliances Corp. of Huntington Beach, Calif.

Red Baby Long Johns – choking risk (2007)

Choking Hazard

The recalled Baby Long Johns are red with snap fasteners down the front and along the legs. A personalized embroidery is stitched across the button-up back flap on the long johns. The long johns were sold in sizes 6, 12, 18 and 24 months.

CPSCJun 7, 2007Nationwide• Li Yi Embroidery Garments Factory, of Guangdong Province, China

Floating Eyeballs (Gemmy) – chemical hazard (2007)

The product is a plastic flashing eyeball toy filled with liquid. The model numbers of this product are: 27828, 27544 and 06470. The model number is found on the back of the packaging. The writing on the packaging reads, "FLASHING EVIL EYE," and "TRY ME!"

CPSCJun 7, 2007Nationwide• Gemmy Industries Corp., of Coppell, Texas

Bayer Healthcare LLC: Ascensia Contour Blood Glucose Monitoring System ( Bayer ...

Incorrect Unit of Measure displayed : The meters report results in the wrong unit of measurement for Canadian users.

FDAJun 6, 2007Nationwide• Bayer Healthcare LLC

Nursery-in-a-Box Cribs – multiple safety risks (2007)

Choking Hazard

The recalled cribs are part of the Nursery-in-a-Box furniture set which also includes a changing table and clothing organizer. The cribs are cherry, white or natural in color. Only model numbers 8910 and 8050 with serial numbers 3005 HY through 0806 HY are included in this recall. The model and serial numbers are printed on an envelope permanently attached to the mattress support. "Simplicity," model and serial numbers are also printed on a label on the bottom rail of the headboard.

CPSCJun 6, 2007Nationwide• Simplicity Inc., of Reading, Pa.

GE Monogram Professional Gas Ranges – fire risk (2007)

Fire/Burn Risk

This recall includes 36-inch and 48-inch stainless steel Monogram Pro ranges with griddles. They are fueled either by LP or natural gas and manufactured from October 2005 through May 16, 2006. The recall includes the following ranges: Models ZDP48N6DHSS, ZDP48L6DHSS, ZDP36N4DHSS and ZDP36L4DHSS. The recalled range models have a serial letter plus serial number combination as shown below. Serial Letter + Serial Number TH + 212588 through 213353 VH + 123456 through 712240 ZH + 210545 through 800064 AL + 200002 through 207337 DL + 200215 through 980416 FL + 202073 through 500677 GL + 000468 through 900468 HL + 202850 through 203252 To find the manufacture date and model and serial numbers, look underneath the top ledge (the "bull nose") above the range controls.

CPSCJun 6, 2007Nationwide• GE Consumer & Industrial, of Louisville, Ky.

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLAB Target Positioner for Leksell Headring used with...

Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings and BrainLAB planning software resulted in a 1.25 mm shift in target area alignment during radiosurgery treatment.

FDAJun 5, 2007OH, WA• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Smiths Medical PM, Inc.: BCI Advisor Vital Signs Monitor (Model/Catalog Number: 9200)

Turn off unexpectedly/ Not turn on : monitors turned off unexpectedly sounding the critical failure alarm. Advisor Vital Signs monitors that were off, would not turn back on.

FDAJun 5, 2007PR• Smiths Medical PM, Inc.

Boston Scientific Corporation One Boston: Boston Scientific Impulse Flextrusion Shaft 5F FR4 16391-...

Labels on the carton from two batches/lots of Impulse Angiographic Catheters may indicate a different curve style than the device that is actually in the carton.

FDAJun 4, 2007Nationwide• Boston Scientific Corporation One Boston

Medtronic Perfusion Systems: Medtronic Performer CPB-Universal R2100375. Catologue N...

Device failure requiring use of back up systems (malfunctioning printed circuit board (PCB))

FDAJun 4, 2007AL, AZ, CA +7 more• Medtronic Perfusion Systems

Quantimetrix Corporation: Quantimetrix QuanTscopics Urine Microscopics Control. Qu...

This recall was initiated due to efficacy concerns with the stabilized erythrocytes, leukocytes and lymphocytes contained in this product group.

FDAJun 1, 2007Nationwide• Quantimetrix Corporation

Quantimetrix Corporation: Quantimetrix SpinalScopics Spinal Fluid Cell Count Contro...

This recall was initiated due to efficacy concerns with the stabilized erythrocytes, leukocytes and lymphocytes contained in this product group.

FDAJun 1, 2007Nationwide• Quantimetrix Corporation