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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

620

Class I (Serious)

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 10241–10260 of 10937 recalls

Medtronic Emergency Response Systems, Inc.: QUIK-COMBO pacing/defibrillation/ECG (therapy) cables use...

Potential for voltage pins in connector of therapy cable to break.

FDASep 2, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 4 inch diameter Roller P...

The pump may stop during the autodose delivery without completion of the dose delivery to the patient.

FDASep 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

Smiths Medical PM, Inc.: Advisor Vital Signs Monitor (model 9200), catalog number ...

Potential Safety related problem associated with the pace detect function on some Advisor monitors that have impedance respiration capabilities in that random pace markers may appear when the pace detect function is turned on and the primary lead is set to Lead II, III or any of the augmented leads, AVL, AVR or AVF on the Advisor monitor.

1...511 512513514 515...547

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FDASep 1, 2005AZ, CA, KS +4 more• Smiths Medical PM, Inc.

Maptangle™ World Edition Floor Mat (Team WorldWide) – Geographic Placement Error (2005)

The floor map game consists of a 6-foot by 5.5-foot vinyl Maptangle™ floor mat that has various multicolored geographic locations and landmarks painted on the floor mat and a set of 103 playing cards, consisting of corresponding geographic locations and landmarks. The object of the game is for a team of players to locate and place their feet on all of the landmarks and geographic locations. The game is age-graded for children 7 years and up. This recall pertains only to the floor mat and does not include any other components of the game. Floor mat map games with manufacture date codes are not subject to this recall.

CPSCAug 25, 2005Nationwide• Team WorldWide Corp., of Taipei City, Taiwan (floor mat only)

Tiki® Bamboo Torches (Lamplight Farms) – Potential Fire Risk (2005)

Fire/Burn Risk

These 5-foot-tall Tiki® bamboo torches consist of a bamboo pole with a weaved basket at the top and a metal flame guard, which is a circular black piece that holds the wick in place and attaches to the fuel canister. The recall includes the Tiki® Beachcomber, Seagrass and Sandpiper model torches. The recall also involves replacement canisters that have the metal flame guards. Recalled units have the following UPC numbers: 086861010372 (Beachcomber), 086861013335 (Seagrass), 086861010457 (Sandpiper) and 076354995262 (Replacement Canister). The UPC number and the model name are written on the packaging or attached tag.

CPSCAug 23, 2005Nationwide• Lamplight Farms Inc., of Menomonee Falls, Wis.

Stork Craft Toy Boxes (Stork Craft) – Manufacturing Flaw (2005)

The recall includes toy boxes with manufacture date codes between November 2002 and July 2004 and the following model numbers and colors: 01520-331 - white, 01520-334 - cherry, 01520-33C - cognac, 01520-33L - oak, and 01520-33N - natural. The manufacture date codes, model numbers, and colors are located on a label underneath the toy boxes. The toy boxes measure 27 inches long by 18 inches wide and 17 inches high. The boxes are constructed of pine.

CPSCAug 19, 2005Nationwide• Stork Craft Manufacturing Inc., of Richmond, British Columbia, Canada

GE Medical Systems, LLC: GE Signa Advantage nuclear magnetic resonance imaging sys...

During use of GE Signa nuclear magnetic resonance imaging system, a flexible Teflon tube that was part of the magnet vent system ruptured and allowed the magnet to vent into the scan room. Because of helium pressure inside the room, the scan room door could not be reopened after the patient was removed from the scan room.

FDAAug 19, 2005Nationwide• GE Medical Systems, LLC

GeoDeck™ Decking (Kadant Composites) – Material Safety Issue (2005)

Laceration Risk

GeoDeck™ is a composite decking product that looks similar to natural wood and is sold in three colors, including: driftwood, cedar and mahogany. The decking materials were manufactured between April 2002 and October 2003. Each decking and railing component has a manufacturing date stamp (day/month/year) on the cut end, which may still be visible on uninstalled materials.

CPSCAug 19, 2005Nationwide• Kadant Composites Inc., of Bedford, Mass.

Philips Medical Systems (Cleveland) Inc: Gemini GXL PET/CT Systems, 6, 10, 16 slice configurations...

The image balance center point correction algorithm used in CT image reconstruction may cause a disapperance or alteration of small circular anatomical structures that are both near the image center and perpendicular to the image plane. This artifact may lead to the misinterpretation of anatomy at the center of the image.

FDAAug 18, 2005IN• Philips Medical Systems (Cleveland) Inc

Bicycle Tires (Torelli Imports) – Potential Rim Failure (2005)

This recall involves Torelli Verona and Lugano Open Tubular bicycle tires with folding Kevlar beads, used to hold the tire to the rim. A red and white label on the sidewall of the Verona model has "Torelli Verona 700 X 23 100-130 psi Handmade Open Tubular" printed on it. A green and white label on the lower edge of the Lugano model has "Torelli Lugano 700 X 23 100-130 psi Handmade Open Tubular" printed on it. The tires are packaged in red and white boxes with the Torelli logo on the front.

CPSCAug 17, 2005Nationwide• Torelli Imports, of Camarillo, Calif.

Holmes® Tower Heater Fans (Holmes Group) – Electrical Safety (2005)

Fire/Burn Risk

The recall involves Holmes® models HFH6498-U, HFH6500-U and HFH6500TG-U and Bionaire® model BFH3530-U. The recalled heaters also have date codes beginning with 2604 through 3804 for all units, except for Holmes® model 6500TG-U, which has date codes ranging from 2604 through 4704. The model and date code can be found on the silver label on the back of the unit. The heater fans are 26 inches tall; come in all gray, two-tone gray, or black and gray; and have either the word Holmes® or Bionaire® printed on the front of the base.

CPSCAug 11, 2005Nationwide• The Holmes Group Inc., of Milford, Mass.

Ritchey Bicycle Wheels (Ritchey Design) – Rear Wheel Issue (2005)

The above wheels were sold by Ritchey as wheel sets and as rear wheel only and as original equipment on 2004 model year Fuji and Motobecane USA bicycles and the 2005 model year Prestige road bike from Raleigh. The recalled wheels have high flange hubs measuring 60 milimeters in diameter and the hub body is straight between the flanges.

CPSCAug 11, 2005Nationwide• Ritchey Design, of San Carlos, Calif. (manufactured under license from American Classic Inc., of Tampa, Fla.)

Trek Diagnostic Systems: VersaTREK Myco AS.

Invitro diagnostic test kit used for testing to confirm the presence of tuberculosis contains interfering bioburden which can cause false positive results.

FDAAug 8, 2005AL, IL, IN +6 more• Trek Diagnostic Systems

Boston Scientific Scimed: Stainless Steel Greenfield Vena Cava Filter with 12 Fr. /...

Certain units within eleven lots of the 12 Fr Greenfield Vena Cava Filter may lack a taper on the braided sheath of the delivery system. The lack of a taper could lead to vessel damage as a result of the sheath catching on the edge of the vein and causing a tear.

FDAAug 5, 2005AL, AK, AZ +31 more• Boston Scientific Scimed

Boston Scientific Scimed: Titanium Greenfield Vena Cava Filter with 12 Fr./4,0 mm ...

FDAAug 5, 2005AL, AK, AZ +31 more• Boston Scientific Scimed

Linvatec Imaging: Linvatec LS 7500, 300 Watt Xenon Light Source Catalog Num...

Through the complaint handling system, the company has determine there are performance issued involving the LS7500, 300 Watt Xenon Light Source. The performance issues result in a low light output that can create poor illumination of the surgical site.

FDAAug 1, 2005Nationwide• Linvatec Imaging

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 6 inch diameter Rolle...

The tube clamp mechanism on the roller pump may not open when the rotation knob is turned, making it difficult to remove and/or insert tubing.

FDAAug 1, 2005GA• Terumo Cardiovascular Systems Corp

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 100V -120V, 15 A (cir...

The power supply may fail to function due to a defective capacitor. (Note; this device incorporates a redundant separate power supply not affected by this capacitor)

FDAAug 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

900 Fusion RMK Snowmobiles (Polaris) – Potential Malfunction (2005)

Fire/Burn Risk

The recall includes model year 2005 Polaris "900 Fusion," "900 RMK," and "900 Switchback" snowmobiles with model numbers: S05PL8DSD, S05PM8DS(A)(B), S05PN8DS, S05PS8DS, S05PM8DS(A)(B)(C), S05PL8DS(A)(B)(C). The snowmobile model and serial number identification decal is located on the right-front side decal of the tunnel. The serial number is permanently stamped into the tunnel and the model number is embossed on the decal.

CPSCJul 28, 2005Nationwide• Polaris Industries Inc., of Medina, Minn.

Greiner VACUETTE North America: Serum Blood Collection Tubes

Serum Blood Collection tubes found with excess of Blood Clot Accelerator (BCA) solution.

FDAJul 28, 2005Nationwide• Greiner VACUETTE North America