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Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment Recalls

All product recalls associated with Medtronic Inc. Cardiac Rhythm Managment.

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Recall Summary

Total Recalls

1000

Past Year

898

Class I (Serious)

125

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 16761–16780 of 17592 recalls

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Protect, model 7285 Dual Chamber Imp...

Medtronic marquis family of ICD and CRT-D devices having batteries manufactured prior to December 2003 that may experience rapid battery depletion due to a specific internal battery short mechanism. Once a short occurs, depletion can take place within a few hours to a few days, after which there is a complete loss of device function.

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Decorative Candleholder (Horn Sing) – fire risk (2005)

Fire/Burn Risk

This recall involves moon, dolphin and fish themed candleholders. The decorative candleholders are about 9 inches tall with a metal bucket that sits suspended from a hook. A votive candle sits inside the bucket.

CPSCFeb 8, 2005Nationwide• Horn Sing Ind. Company Ltd., of Taipei, Taiwan

Bausch & Lomb Inc: SofLens 66 Toric Visibility Tinted Contact Lenses for Dai...

1...837 838839840 841...880

Page 839 of 880Next

Portion of lot contains lenses with incorrect refractive power.

FDAFeb 4, 2005Nationwide• Bausch & Lomb Inc

Varian Medical Systems Inc 3100 Hansen Way M/S E-210 Palo Alto CA 94304-1030: Varian brand Clinac 600C (CD, EX) and Portal Vison with D...

Treatment beam may not completely pause while device changes field shape; Potential for mistreatment could occur.

FDAFeb 4, 2005IN• Varian Medical Systems Inc 3100 Hansen Way M/S E-210 Palo Alto CA 94304-1030

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 AED.

Potential to not detect patients at the low end of the patient impedance range.

FDAFeb 3, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Snowboard Bindings (Rossignol/Dynastar) – safety failure (2005)

This recall includes all 2003/2004 model year Rossignol-brand HC 500, Zena, Unit Pack, HC Rental, and Unit Rental snowboard bindings. Also included are the 2003/2004 model year Dynastar-brand Classic RL and Classic Pack snowboard bindings. This recall does not involve current products (2004-2005) or other models.

CPSCFeb 1, 2005Nationwide• Rossignol Ski Company, Inc. and Skis Dynastar, Inc. of Williston, Vermont

DR Leaf and Lawn Vacuum (Country Home) – operational issue (2005)

The recalled vacuum is designed to be pulled behind a lawn tractor. The product vacuums leaves and grass, shreds them and collects the shredded material in a large storage chamber. The leaf and lawn vacuums have a red circle with DR printed in black on each side of the chamber.

CPSCFeb 1, 2005Nationwide• Country Home Products, Inc. of Vergennes, Vt.

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

System 1 power supply may electrically short to the main console, disrupting normal system operation by causing unexpected re-setting or shutdown of pumps and modules, false alarms and/or overheating and failure of the central control monitor.

FDAFeb 1, 2005Nationwide• Terumo Cardiovascular Systems Corp

Guidant Corporation Advanced CardiovascularSystem: Voyager RX Coronary Dilatation Catheter

Leak at guide wire exit notch could introduce air into the artery.

FDAJan 27, 2005IN• Guidant Corporation Advanced CardiovascularSystem

HD Designs 5-piece Dining Set (Commend Co.) – Structural Weakness (2005)

The chairs and table are sold unassembled as part of a boxed 5-piece dining set. The words "HD Designs 5 Piece Dining Set" and item number BFR3917HO are written on the box. The chairs and dining table are honey oak wood and the seats have beige vinyl padding.

CPSCJan 26, 2005Nationwide• Commend Co. Ltd., of Fair Lawn, N.J.

GE OEC Medical Systems, Inc: InstaTrak 3500 Plus system with cranial application (aid ...

Tracking inaccuracy of 5-10 mm may result when the shunt guide accessory is used with version 5.1 software.

FDAJan 26, 2005AL, AK, AZ +21 more• GE OEC Medical Systems, Inc

Jumpking Trampolines (Jumpking Inc.) – Potential Injury Risk (2005)

Laceration Risk

The recall includes 14-foot and 15-foot Jumpking trampolines sold separately and with FunRing enclosures. The brand name "Jumpking, Inc." is written on a warning label wrapped around a leg of the trampoline. The eight legs of these trampolines fit into perpendicular sockets welded to the top rails. Trampolines with weldless sockets that fit over the connecting top rail pieces are not included in this recall. The FunRing enclosures have an arched design where the vertical poles are connected by arches at the top. Some enclosures were sold separately from the trampolines. Later units, that include the rubber sleeves that fit around the mounting brackets, are not included in the recall.

CPSCJan 25, 2005Nationwide• Jumpking Inc.® of Mesquite, Texas

Aprilaire Electronic Air Cleaners (Research Products) – Performance Issue (2005)

Fire/Burn Risk

The recall involves all Aprilaire Model 5000 Electronic Air Cleaners. The air cleaners are almond colored and are located near the heating and cooling equipment. An identification label on the access door reads "Aprilaire Model 5000."

CPSCJan 24, 2005Nationwide• Research Products Corp., of Madison, Wis.

Fun Years Music Big Drum Set (Kids Station) – Potential Injury (2005)

Choking Hazard

The recalled music set includes a yellow and green drum with a clear plastic lid and a red one-piece carrying strap that doubles as a storage and carrying case for additional instruments. The drum measures 12 inches in diameter and about 7.5 inches in height. The instruments stored in the drum include: purple drumsticks, yellow and red dumb-bell-shaped maracas, purple wrist bells, an orange recorder, a yellow harmonica, a red-rimmed tambourine and a yellow whistle. Only this musical set is part of this recall. A similar drum set sold at Toys "R" Us with a two-piece strap and different musical toys is manufactured by a different company and is not being recalled.

CPSCJan 19, 2005Nationwide• Kids Station Inc., of Miami, Fla., for Toys "R" Us, of Wayne, N.J.

North Coast Medi-Tek Inc: SourceOne Healthcare Technologies brand, Ultrasound Tray,...

Outside box labeling, containing 10 trays, incorrectly identified the product as ultrasound trays. Product is Breast Biopsy trays, Cat. 255826R2. Individual tray package labeling correctly identifies the product as Breast Biopsy tray.

FDAJan 18, 2005OH• North Coast Medi-Tek Inc

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

The LIFEPAK 12 biphasic defibrillator/ monitors may deliver inappropriate energy levels and fail to escalate energy levels when configured to do so.

FDAJan 15, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

40-Watt Mini Spotlight Bulbs (Comtrad) – Fire Risk (2005)

Laceration Risk

The recalled 40-Watt "Type R" incandescent mini spot-light bulbs were included in two- and three-lamp accent lights in certain furniture hutch items manufactured by Sauder Woodworking Co. The furniture hutch models involved are: Model 9386 - Uses the three-lamp kit Model 9549 - Uses the two-lamp kit Model 9509 - Uses the two-lamp kit

CPSCJan 13, 2005Nationwide• Comtrad, Division of Waljon Ltd., Mississauga, Ontario, Canada

Ridgid 16-Gallon Blower Vac (Emerson Tool) – Operational Risk (2005)

Laceration Risk

The Ridgid® 16-gallon 2-in-1 Blower Vac, Model WD16650, has light gray drums with orange lids, gray power heads, and black wheels. The recalled units have the model number and a serial number from 04104C through 04114C located on a label on the side of the power head. "Ridgid® 2 in 1 Blower Vac" is written on the front of the units.

CPSCJan 13, 2005Nationwide• Emerson Tool Co., of St. Louis, Mo.

Mammut Barryvox Avalanche Transceivers – Technical Malfunction (2005)

The recalled Barryvoxes are 2004/2005 model Opto 3000 Avalanche Transceivers. The words, "Mammut" and "Barryvox" are printed on the front of the red and black transceivers. The serial numbers on the recalled units, which can be found in the battery compartment under the UPC code, include: M0080000 through M0088419, M0089616 through M0089800 and M0090000 through M0090419. The recalled units were shipped with an instructional CD and the box marked "Bonus CD Included." Units containing safe replacement transceivers have a red triangular label reading "New Casing" on the box.

CPSCJan 13, 2005Nationwide• Ascom Systec AG, Eichtal, of Switzerland

Fischer Imaging Corporation: Bloom DTU-215-B Programmable Stimulator

Possibility that after a loss of power or brown-out, the device may transmit unintended stimulation to patients.

FDAJan 13, 2005Nationwide• Fischer Imaging Corporation