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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

583

Class I (Serious)

91

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 9761–9780 of 10937 recalls

Medtronic Emergency Response Systems, Inc.: Batteries used with the LIFEPAK 20 defibrillator/monitor

Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on backup (DC) battery power.

FDAMar 30, 2007IN• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 defibrillator/monitor. The device is an AC po...

Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on backup (DC) battery power.

FDAMar 30, 2007IN• Medtronic Emergency Response Systems, Inc.

Electric Mobility Corp: Rascal Scooters with Electric seat lifts, Model 600 Serie...

Seat and/or lift actuator problems: 1) Models equipped with a Seat Lift, the mast screw and washer holding the Seat Lift Actuator in place will loosen break off or fall out; 2) Models assembled with Seat Lift Actuator or Seat Post Mounting Bolts, the seat may wobble or the seat will break off from the vehicle; 3) Models using Seat-On Lifting brackets with a hoist to raise an EMC vehicle equipped w

1...487 488489490 491...547

Page 489 of 547Next

FDAMar 29, 2007Nationwide• Electric Mobility Corp

Binax, Inc. dba IMPD: BinaxNOW A&B Kit 10 Test Kit (Japan) Part No. 416-110J ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Influenza A&B 22 Test Kit Part Number: 416-022, ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Nasopharyngeal (NP) Accessory Pak, Part Number 4...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Binax, Inc. dba IMPD: BinaxNOW Influenza A&B 10 Test KIT Part Number: 416-110 ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

Triax PK7 Bicycles (Shun Lu) – Frame Failure (2007)

This recall involves Triax PK7 (model 8509-24) and Vertical PK7 (model 8596-71T) 20-inch aluminum cushion framed bicycles. The Triax model was manufactured between November 2005 and October 2006, and the Vertical model was manufactured between August 2004 and December 2004. The model numbers and manufacture dates are printed on a label affixed to the bicycle frame.

CPSCMar 28, 2007Nationwide• Shun Lu Bicycle Company, of Guangdong, China

Binax, Inc. dba IMPD: BinaxNOW RSV 10 Test Kit Part Number : 430-100, contains ...

Tip of the foam swab could detach from the shaft causing injury to the patient.

FDAMar 28, 2007Nationwide• Binax, Inc. dba IMPD

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usage...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Designe...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: UroView 2800; MDL number A349855. Product Usage: Desig...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product ...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC 9800 Plus Digital; MDL number A349855. Product Usa...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

Class IIModerate

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC MiniView 6800 Mobile; MDL number A349855. Product Us...

Please be aware that this is not a new recall. The firm has taken action; but, due to administrative issues this recall is now being classified by the Agency. GE OEC had discovered an issue with the hard disk drives that were installed on OEC device models: UroView 2800; 9800 Plus Digital; MiniView 6800; and FlexiView 8800 Mobile C-Arm. The devices were manufactured between October 15, 2004 and

FDAMar 27, 2007Nationwide• GE OEC Medical Systems, Inc

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic ...

Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 4100/4100 IQ. Digital Fluoroscopic ...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging...

Caution on the non-detection of small invasive objects/devices, which project out from the skin surfaces (e.g. biopsy or other needles) while using the Innova Sense software option designed for patient contouring. Usage of Innova Sense patient contouring for such devices could potentially lead to patient injury.

FDAMar 26, 2007Nationwide• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC

General Electric Med Systems LLC: GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imagin...

Measurement errors during the computation of vessel diameters while using the Stenosis Analysis software (also known as Quantitative Coronary Analysis function-QCA) using the auto-calibration function on Innova Digital (located in control room) or in-room InnovaCentral/Touch-Screen

FDAMar 26, 2007AZ, CA, CO +22 more• General Electric Med Systems LLC