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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)

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 19561–19580 of 21319 recalls

Medtronic Emergency Response Systems, Inc.: LIFEPAK 12 defibrillator/monitor

Therapy connectors may have connector sockets that do not meet design specs - short drill depth. Interruption of the connections may cause unexpected, intermittent or complete loss of pacing and defibrillation functions.

FDAMar 22, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Fresenius Medical Care North America: Newton IQ 4 Lead Cycler Set with stay-safe patient connec...

Stay safe trigger body may not connect to the extension set and result in associated peritonitis

FDAMar 22, 2006Nationwide• Fresenius Medical Care North America

Radiometer America Inc: Capillary (end) caps, accessory for use with blood gas an...

Capilliary end caps, an accessory for ABL blood gas analyzers, leak blood from capillary tubes during transport.

1...977 978979980 981...1066

Page 979 of 1066Next

FDA

Mar 22, 2006

Nationwide

• Radiometer America Inc

Excelsior Medical Corp: ESP 140 Syringe Pump. Used for medication infusion. Mod...

Potential for alarm failure when the 140 pump completes infusion and/or the pump encounters a mid-infusion occlusion, when used in the 140 mode with a 140cc syringe. The ESP Pump works correctly when used in 60 mode with a 60cc syringe or smaller.

FDAMar 21, 2006Nationwide• Excelsior Medical Corp

Respironics California Inc: Ventilator-PLV Continuum (PLVC I), Model Number: P1000....

Flow valve failures- When failure occurs, air flow from the ventilator ceases resulting in the PLVC I transitioning into a 'Vent Inop' mode whereby the safety valve is activated, opening the circuit to ambient air. Ventilator dependent patients may not receive adequate ventilatory support if this problem occurs.

FDAMar 20, 2006Nationwide• Respironics California Inc

Hitachi Medical Systems America Inc: MRP-7000, AIRIS Magnetic Resonance Imaging Systems

Software anomaly. A software defect in the referenced systems can cause a slice indicator (reference line) to be mis-positioned on the cross-reference image when it is magnified. This image error could result in a possible patient mis-diagnosis.

FDAMar 17, 2006Nationwide• Hitachi Medical Systems America Inc

Vanguard Medical Concepts, Inc: Product is Reprocessed Ethicon Bladeless Trocars. Model: ...

Review of complaints and testing show that the distal tip of the trocars may separate while in use.

FDAMar 17, 2006Nationwide• Vanguard Medical Concepts, Inc

Siemens Medical Solutions USA, Inc: SOMATOM Sensation CT Systems

Firm became aware of a potential problem that could affect scan results and require patient exam to be repeated when using the customized ECG-gated scan protocols in the CT2006A and CT2006G software of their SOMATOM Sensation CT Systems.

FDAMar 17, 2006Nationwide• Siemens Medical Solutions USA, Inc

Kinetic Concepts, Inc: Sterile packaged wound dressing with white and green inne...

Complaints received regarding difficulty opening the nonadherent layer of the device prior to application to open abdominal wounds.

FDAMar 17, 2006Nationwide• Kinetic Concepts, Inc

Walgreens Iron Supplement (Inverness) – Potential Contamination (2006)

The recalled supplements were sold in a brown plastic bottle. "Walgreens Finest High Potency Iron Supplement" is printed on the yellow and green label on the bottle.

CPSCMar 16, 2006Nationwide• Inverness Medical Nutritionals Group, of Freehold, N.J.

Plasma Flat Panel TVs (Philips) – Potential Defect (2006)

The recall involves only certain 42- and 50-inch, 2005 model Philips branded Plasma Flat Panel Televisions with Ambilight technology, which is an ambient lighting feature that projects a soft light onto the wall behind the TV to enhance the display. They were manufactured with the following model, date codes, and serial numbers: Model Display Type Production Began Production Ended Beginning Serial Range Ending Serial Range 42PF9630A/37 Plasma April 2005 July 2005 AG1A0518xxxxxx AG1A0528xxxxxx 50PF9630A/37 Plasma May 2005 August 2005 AG1A0519xxxxxx AG1A0533xxxxxx 50PF9630A/37 Plasma June 2005 August 2005 YA1A0523xxxxxx YA1A0534xxxxxx 50PF9830A/37 Plasma June 2005 August 2005 AG1A0526xxxxxx AG1A0533xxxxxx The model and serial numbers can be found on the back of the TV on the label that looks like the example in the picture: The serial number can also be obtained by pushing the following keystrokes on the remote control: 123654, after which a customer service menu ("CSM") will be displayed on the screen. In the menu, line 03 displays the type number and line 04 displays the production code (identical to the serial number of the set). Press the MENU button on the remote to exit the CSM.

CPSCMar 16, 2006Nationwide• Philips Consumer Electronics North America, of Atlanta, Ga.

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

LIFEPAK 20 may lock-up when attempting to power-up on DC within 2 seconds after removing AC power.

FDAMar 16, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Bayer Healthcare, LLC (Diagnostics Division): ADVIA 2120 systems -Automated Complete Blood Cell and Dif...

The ADVIA 2120 has reported ; highly intermittent low results on all primary results: White Blood Cells (WBC), Red Blood Cells (RBC), Hemoglobin (HGB) and Platelets (PLT) and an abnormal baso cytogram.

FDAMar 16, 2006Nationwide• Bayer Healthcare, LLC (Diagnostics Division)

B & K Medical Systems, Inc.: Convex Array Transducer used with B-K Ultrasound Scanners...

Due to a problem with calibration, the device can produce up to 50% elevated acoustic output and up to 2 degrees higher surface temperature

FDAMar 16, 2006CA, CT, FL +10 more• B & K Medical Systems, Inc.

Hobbs Medical, Inc.: Hobbs Medical 3 Prong Looped Retriever, a disposable devi...

Diameter of device at the distal end would prevent it from passing through the endoscope's working channel.

FDAMar 15, 2006AK, IA, KY +5 more• Hobbs Medical, Inc.

Olympus 35mm Film Cameras – Overheating Risk (2006)

Fire/Burn Risk

The recall includes the Infinity Twin, AF-1 Twin, Infinity Zoom 200 series, AZ 200 series, and Quantary Infinity Zoom 222 Olympus-brand 35mm film cameras. The model name is printed on the face of the camera. These cameras have a built-in flash.

CPSCMar 14, 2006Nationwide• Olympus America Inc., of Melville, N.Y.

Stryker Howmedica Osteonics Corp.: Trident PSL Acetabular Shell;Arc Deposited;Hydroxylapatit...

Dimensional anomaly

FDAMar 13, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Documentation Cart with Articulating Arm, Model Num...

THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.

FDAMar 10, 2006Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141: Access Point Medical Canes, Cane, Off-Set Crook w/Strap-B...

The canes were made of unacceptable materials and could break

FDAMar 10, 2006Nationwide• Access Point Medical LLC Three City Place Drive Suite 750 St. Louis MO 63141

Apple Medical Corporation: Fischer Cone Biopsy Excisor - Small Model: 900-150

Fire/Burn Risk

Change in product material may be cause for wire breaking, and tip burning and melting during procedure. Broken pieces of the device may need to be retrieved from patient.

FDAMar 10, 2006Nationwide• Apple Medical Corporation