Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc. Recalls

All product recalls associated with Medtronic Emergency Response Systems, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

426

Class I (Serious)

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 4241–4260 of 4598 recalls

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Biogenex Laboratories: Super Sensitive Link-Label IHC Detection System/Mega Volu...

Mislabeling: The product's "contents section " labeling (outer box) is mislabeled incorrectly printed as '1 x 100 mL Alk Phos Label' which should read '1 x 100 mL HRP Label'. A second, smaller label, incorrectly reads "RTU MultiLink HPR/AEC" which should be labeled as "RTU MultiLink HPR". The reagent vials in the box are correctly labeled.

FDA

1...211 212213214 215...230

Page 213 of 230Next

Oct 3, 2006

• Biogenex Laboratories

Draeger Medical, Inc.: Fabius GS Anesthesia Machine. Catalog number 8604699

One of four casters may break loose from chassis

FDAOct 3, 2006Nationwide• Draeger Medical, Inc.

GE OEC Medical Systems, Inc: OEC 9900 Elite Fluoroscopy System, Catalog No. 887208 and...

X-ray system may lose or mix images and/or lose patient data.

FDASep 30, 2006Nationwide• GE OEC Medical Systems, Inc

Organogenesis, Inc.: Apligraf (Graftskin)

Product pH out of specification

FDASep 29, 2006Nationwide• Organogenesis, Inc.

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

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. On October 11, 2006, GE Healthcare recalled GE OEC InstaTrak 3500 Plus System with Software version 5.2, the surgical Navigation and Visualization Application due to software related issues.

Class IHigh

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: InstaTrak with Multiple Dataset Navigation, 892.2050 Syst...

FDASep 15, 2006Nationwide• GE OEC Medical Systems, Inc

True Religion Hoodie – Strangulation Risk (2006)

The recalled hoodies have a drawstring through the hood. The products are black, pink, or blue and were sold in children's sizes XS, S, M, L, and XL. The True Religion horseshoe design is displayed on the front of the hoodie. The name "True Religion" appears inside the hoodie.

CPSCSep 14, 2006Nationwide• True Religion, of Los Angeles, Calif.

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Fluoroscopy System with Integrated Navi...

Missing, mixed or lost patient images may result after X-ray procedures. Error in navigation accuracy.

FDASep 13, 2006FL, GA, IL +11 more• GE OEC Medical Systems, Inc

Biogenex Laboratories: Anti-CD45 Cocktail antibody in 6 ml vials; Cat. No. AM371...

Mislabeling: Anti-CD45 cocktail antibody mislabeled as Ki-67.

FDASep 5, 2006TX• Biogenex Laboratories

Conmed Electrosurgery: Conmed System 5000 Electrosurgical unit, REF 60-8005-SYS,...

Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.

FDASep 5, 2006Nationwide• Conmed Electrosurgery

Conmed Electrosurgery: Conmed System 2500 Electrosurgical Unit, REF 60-8011-SYS,...

Wrong size capacitor installed in electrosurgical generator could malfunction, causing muscle stimulation or delay in therapy.

FDASep 5, 2006Nationwide• Conmed Electrosurgery

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 external defibrillator/monitor

Devices with v38 system software do not display a ''LOW BATTERY: CONNECT TO AC POWER'' message when the monitor is on backup (DC) battery power and may shut down without warning.

FDAAug 30, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

GE OEC Medical Systems, Inc: GE OEC 9800 Fluoro C-Arm X-ray System, GE OEC Medical Sys...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE O...

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: RUS Tool Version Software

X-ray systems could provide output which exceeds the 20 R/minute limit.

FDAAug 16, 2006Nationwide• GE OEC Medical Systems, Inc

Ge Healthcare: GE ApexPro CH Telemetry System. The ApexPro Telemetry Sy...

When a patient being monitored with ApexPro/Apex Pro CH Telemetry with ST monitoring disabled is in a pre-existing condition of continuous MESSAGE or ADVISORY level alarm preceding a SYSTEM WARNING level alarm, the SYSTEM WARNING audible alarm and flashing yellow border around the patient panel at the CIC (Clinical Information Center) does not occur.

FDAAug 4, 2006PR• Ge Healthcare

Generac GTH Engines – fuel tank fire risk (2006)

Fire/Burn Risk

The following industrial power equipment products, manufactured by the original equipment manufacturers (OEMs) listed below, are included in this recall: Power Equipment Type OEM/Equipment Seller Pressure Washer Cleaning Systems Specialists, Inc. Phone: (619) 448-8111 Air Compressors Ingersoll-Rand Phone: (800) 820-0308 Pressure Washers Silver Eagle Phone: (936) 264-2215 Saw Mill Wood Mizer Phone: (317) 808-0717 The recalled Generac GTH410 and GTH220 engines were manufactured from July 2001 to July 2005. GTH410 Engines model numbers with defective fuel tanks are: 0041930EHF; 0043290EHF; 0043291; 0045050EHF; 0045281; 0045283; 0046100EHF; 0046150EHF; 0046910EHF; 0046911. GTH220 Engines model numbers with defective fuel tanks are: 0040990EHC; 0043930EHC; 0045300EHC; 0046090EHC; 0046370EHC; 0046380EHC; 0046390EHC; 0046820EHC; 0047640EHC; 0048820; 0050650; 0051170. The engine model number is located on the side of the motor and contained on a small sticker above the Generac nameplate. The top number on the small sticker is the model number (e.g., 220 or 410). The larger Generac nameplate contains the Engine Identification Number and Serial Number.

CPSCJul 27, 2006Nationwide• Generac Power Systems Inc., of Waukesha, Wis.

Ge Healthcare: ApexPro FH Telemetry System: composed of six major compon...

System Warning Alarm failure: When a patient being monitored is in a pre-existing condition of continuous MESSAGE or ADVISORY level alarm preceding a SYSTEM WARNING level alarm, the SYSTEM WARNING audible alarm and flashing yellow border around the patient panel at the CIC does not occur.

FDAJun 23, 2006Nationwide• Ge Healthcare