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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 35361–35380 of 37665 recalls

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

The defibrillator may not operate if the device is turned on during an AC Loss Alert.

FDAJun 17, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Boston Scientific CRM Corp: VENTAK PRIZM AVT model no. 1900, Atrial and Ventricular T...

The atrial therapy (AVT) subgroups of certain Guidant ICD and CRT-D product families are subject to a condition in which a random memory error causes functional 'latching' that limits available therapy.

FDAJun 17, 2005Nationwide• Boston Scientific CRM Corp

Radiometer America Inc: Blood Gas and Co-Ox Electrolyte & Metabolyte Analyzer, AB...

Software defect. pO2 and pCO2 sample test results run on the firm's ABL700/800 Series Blood Gas Analyzers are not being properly flagged during the sample calibration phase.

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FDA

Jun 17, 2005

Nationwide

• Radiometer America Inc

Radiometer America Inc: D711, Reference Membranes, Part #942-058, used with the A...

The recalled membranes cause the status value of the pH and electrolyte electrodes to be offset causing readings outside of the acceptable range.

FDAJun 17, 2005Nationwide• Radiometer America Inc

Boston Scientific CRM Corp: CONTACT RENEWAL 3 AVT model numbers M150 and M155; CONT...

FDAJun 17, 2005Nationwide• Boston Scientific CRM Corp

Boston Scientific CRM Corp: VITALITY AVT, model A135 and model A155. Implantable Car...

FDAJun 17, 2005Nationwide• Boston Scientific CRM Corp

Datascope Corp: Panorama Patient Monitoring Network. Cardiac Arrhythmia ...

Upon the new release of software, the firm started receiving reports of unexpected system failures in the database subsystem related to virtual memory pages.

FDAJun 16, 2005Nationwide• Datascope Corp

Baxter Healthcare Corp. Rt.: Baxter''s Patient Care System (BPCS) software, composed o...

If a pharmacy end user alters the Administration Unit of Measure (AUOM) of an ordered drug, the AUOM will display incorrectly on the Medication Administration Record for the patient, possibly leading to medication errors.

FDAJun 16, 2005CA, MA, MO +1 more• Baxter Healthcare Corp. Rt.

Baby Connection Fun Frog Soft Gym (Infantino) – safety risk (2005)

Laceration Risk

The recalled Baby Connection Fun Frog Soft Gym is comprised of a multi-colored, frog-shaped padded fabric mat, from which blue and orange support arms extend. The support arms consist of thin steel wire covered by foam and fabric. They can be arched, allowing for three stuffed infant toys to hang above the product's mat. A label with the word "Infantino" is attached to each of the stuffed toys as well as the underside of the mat. Products sold under item 150-761, Infantino Activity Soft Gym, which have a stamp on the back of the product showing 150-761 Production Date June 2005, are not affected by this recall.

CPSCJun 15, 2005Nationwide• Infantino LLC, of San Diego, Calif.

Jøtul Gas-Fired Stoves – potential malfunction (2005)

Fire/Burn Risk

The recall involves two Jøtul models of gas-fired stoves - the GF 100 DV II Nordic QT and the GF 200 DV II Lillehammer. The stoves are fueled with liquid propane (LP) gas. The model number (either GF 100 DV II or GF 200 DV II) can be found on the metal rating plate attached to the back of the stove.

CPSCJun 14, 2005Nationwide• Jøtul North America, of Portland, Maine

Qualitest Pharmaceuticals Inc: AccuSure Insulin Syringe, 1cc, 28 guage, 1/2'', packaged ...

Labeling error. There is a possibility that 1cc syringes are labeled at 1/2cc on the plastic inner wrap holding bundles of 10 syringes.

FDAJun 14, 2005Nationwide• Qualitest Pharmaceuticals Inc

Baxter Healthcare Renal Div: Baxter Arena Hemodialysis Systems, product codes ARENADPX...

Operator's Manuals addenda are being issued to provide correct information concerning the correct syringe size to use for heparin infusion, the use of chemical disinfectants in the System 1000, TMP Advise, and Bicarbonate Value calculations.

FDAJun 14, 2005Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Renal Div: Baxter System 1000 Single Patient Hemodialysis Systems, p...

FDAJun 14, 2005Nationwide• Baxter Healthcare Renal Div

Fire Stick Multi-Purpose Lighters (Aristo) – safety risk (2005)

Fire/Burn Risk

These refillable butane-fueled lighters are silver in color with a black sliding switch at the middle of the product. Two models of the lighters are included in this recall: a 7-inch model (model number 324007) and a 12-inch model (model number 324012). "Aristo Home & Garden" and "Fire Stick" are printed on the products' original packaging.

CPSCJun 13, 2005Nationwide• Aristo Home and Garden, of West Deptford, N.J.

H.E.B. Vitamins (Perrigo) – product safety (2005)

The recalled H.E.B. Super B-Complex vitamins with iron and 300 mg Vitamin C was sold in a container of 80 caplets. The white plastic bottle is labeled, "H.E.B. and Super B-Complex with Iron and 300 mg Vitamin C" and "Energy Metabolism" and has a blue lid.

CPSCJun 13, 2005Nationwide• The Perrigo Co. of South Carolina, of Greenville, S.C.

Baxter Healthcare Corp. Rt.: Baxter 6060E Epidural Infusion Pump, product code 2L9351 ...

There is an overinfusion condition in the Intermittent mode where the pump may continue to deliver at the higher dose rate instead of switching to the lower keep open rate once the first dose is completed.

FDAJun 13, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter 6060 Multi-Therapy Infusion Pump, product code 2M9...

FDAJun 13, 2005Nationwide• Baxter Healthcare Corp. Rt.

Bunn Home Coffeemakers – electrical issue (2005)

Fire/Burn Risk

The recall involves Bunn® home coffeemakers with model numbers GR-10B, GR-10W, B-10B, B-10W, and BT-10B (including any of those same model numbers ending in the additional letter D) with six-digit date codes ending in "01," "02," or "03." Also involved in the recall are the same models with dates codes ending in "04" and middle digits between "01" and "21." (If the date code has a seventh digit, consumers should ignore the last digit and use the first six digits.) The model number and date code are stamped on a small white or silver sticker on the bottom of the coffeemaker. The 10-cup Bunn® coffeemakers have either a black or white plastic base and top, and measure 14¼ inches high by 7 inches wide by 13¾ inches deep. The word "BUNN®" is printed on the front of the machine in chrome.

CPSCJun 10, 2005Nationwide• Bunn-O-Matic Corp., of Springfield, Ill.

Del Laboratories Inc.: Orajel toddler EXTRA GENTLE Yellow Manual Toothbrush, Mod...

Choking Hazard

Firm received several consumer complaints that the elastomer head of the toothbrush had separated (broke) from the handle during use and could pose a choking hazard to children.

FDAJun 9, 2005Nationwide• Del Laboratories Inc.

Radiometer America Inc: ABL 5 Capillary Adaptor (a connection that fits the capil...

The dimensions and shape of the analyzer adaptor do not fit the analyzer tubes or probe, causing air to be aspirated with the blood sample and causing a deviation in the pO2 sample results.

FDAJun 9, 2005Nationwide• Radiometer America Inc