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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

593

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 9381–9400 of 10391 recalls

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Adjustable Valve, 6248VAL, Sterilized using irr...

Medtronic has identified an issue with the packaging for specific lots of the Medtronic Adjustable Valve and valves contained in the Attain Left Heart Delivery System kits. A small number of valve package seals could be compromised.

FDAAug 27, 2008GA, OR, RI +3 more• Medtronic Inc. Cardiac Rhythm Managment

Indoor Lighting Fixtures (Lithonia) – Impact Hazard (2008)

The recall involves the Hi-Bay Indoor High-Intensity Discharge (HID) Fixtures, model numbers PG16A and PG21A. The fixture is intended for high-mounting heights (at least 20 feet above floor level) and is used in retail, warehouse and heavy manufacturing locations. The fixture's housing is made of die-cast aluminum.

CPSCAug 27, 2008Nationwide• Lithonia Lighting, of Conyers, Ga.

Philips Medical Systems North America Co. Phillips: Allura Xper FD10 Monoplane X-ray system. Intended for use...

Due to a potential geometry software lock up during a Digital Rotational Angiography (DRA) run, the stand and table movement may no longer be possible.

1...468 469470471 472...520

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FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Philips Medical Systems North America Co. Phillips: Allura Xper FD10/10 Biplane X-ray system. Intended for us...

Potential for table and stand not to move due to a software error.

FDAAug 21, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Wolf SL Carbon Bicycle Forks (True Temper) – Fall Hazard (2008)

The recalled forks have a clear coating over black painted carbon fiber, with the words "Wolf Superlite" and related logo just below the crown on each fork leg, and the letters "SL" on each leg above the fork blade dropouts. There is a True Temper CRT™ logo on the inside of both fork legs. The recalled forks could have been included on the following bicycle models: R3, R3 SL, Soloist Carbon, Soloist Carbon SL, and certain P3 Carbon framesets and complete bicycles.

CPSCAug 20, 2008Nationwide• True Temper Composite Material Products Co. Ltd, of Guangzhou, China

Philips Medical Systems North America Co. Phillips: Essenta DR is a digital multifunctional X-ray systems, su...

When a patient is selected in the patient list and examination tab pressed with background query running at the same time, the wrong patient may be selected.

FDAAug 15, 2008Nationwide• Philips Medical Systems North America Co. Phillips

Smith & Nephew, Inc. Endoscopy Division: DYONICS 25 Fluid Management System bag for enclosure of w...

Integrity of the remote control bag may not be sufficient to prevent tearing or opening of the bag during use.

FDAAug 7, 2008PR• Smith & Nephew, Inc. Endoscopy Division

Smith And Nephew, Inc. Wound Management Division: GlobTek, Inc. Power Supply for Medical Use Part No: TR9CE...

External battery chargers used with the Version 29 VISTA Negative Pressure Wound Therapy pumps are failing to properly charge the pump's battery.

FDAAug 7, 2008Nationwide• Smith And Nephew, Inc. Wound Management Division

Smith & Nephew Inc: Caption Disposable Platelet Concentrator Kit, Ref 711782...

Product contained a syringe whose package seal integrity can be adversely affected when the product is exposed to low atmospheric pressure. This may occur during shipping.

FDAAug 5, 2008Nationwide• Smith & Nephew Inc

Wooden Cribs (Mother Hubbard's) - Fall Risk (2008)

The recall includes the following wooden full-size cribs: "Enchantment" (model #210), "Hush a Bye" (model #215), "Once upon a time" (model #320) and "Rock a bye" (model #1900-350). Only date codes from 0306 through 0308 are included in this recall. "Mother Hubbard's Cupboards", the model number and date code are printed on a label located on the bottom inside of the right side.

CPSCAug 5, 2008Nationwide• Mother Hubbard's Cupboards, of Toronto, Canada

Wooden Toys (Earthentree) - Choking Risk (2008)

Choking Hazard

This recall involves a variety of wooden toys including egg shakers (maracas), pull toys, rattles, and trains. The toys are painted glossy red, orange, green, brown, yellow or natural wood.

CPSCJul 29, 2008Nationwide• Earthentree of Kirkland, Wash.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo II VR D284VRC, for ventricular pacing an...

Maximo II VR ICD, DR ICD and CRT-D inadvertently include the Capture Management algorithm (Atrial/Right Ventricular/Left Ventricular Capture management). The Capture management algorithm monitors daily pacing thresholds and may increase or decrease pacing amplitudes in response to patients' needs. Although the algorithm is operating correctly, it is not accessible to the clinician for reprogramm

FDAJul 25, 2008Nationwide• Medtronic Inc. Cardiac Rhythm Managment

GE Healthcare: Innova 4100 / 4100 IQ , GE Healthcare, Waukesha, WI 53188...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

Medtronic Inc. Cardiac Rhythm Managment: Maximo II CRT D284TRK, for ventricular pacing and defibri...

FDAJul 25, 2008Nationwide• Medtronic Inc. Cardiac Rhythm Managment

GE Healthcare: Innova 2100IQ (The Digital Fluoroscopic Imaging System co...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

GE Healthcare: Innova 2000; The principle system components include a C-...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

GE Healthcare: Innova 3100 / 3100 IQ, Cardiovascular Imaging System, GE ...

The charger and / or battery of the PDB may fail earlier than expected with no advance warning and thus cause the system to shut down.

FDAJul 25, 2008Nationwide• GE Healthcare

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo II DR D28DRG, for ventricular pacing an...

FDAJul 25, 2008Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Dirt Devil Power Brush Attachment – Laceration Risk (2008)

Laceration Risk

The recalled Dirt Devil Turbo Tool/Power Brush attachment was sold as an accessory with the following Dirt Devil vacuum models. Only vacuum tool accessories with date codes J7060 through J7365 and have a C-clip connector are included in this recall. The date code is located on the underside of the vacuum accessory. The Turbo Tool/Power Brush tools are about 6 ½ inches long by about 5 inches wide and come in a variety of colors that match the color of the vacuum. The housing of the tool was made in clear, red, green, or light blue with clear, light blue, dark blue, red, purple, or black turbine fans with matching brush rolls. Dirt Devil Vacuum Models Reaction Purpose for Pets Ultra Swivel Glide M110000 M140000 M086020 M110000HD M140000CA M110001B M110002 Envision Wide Glide Swerve M110003 M086700WCA M086030 M110006 M086710 M086030CA M110008 M110008CA Action Upright Royal Commercial M110009 M110020CAB RY6100

CPSCJul 23, 2008Nationwide• TTI Floor Care North America, of Glenwillow, Ohio

Walther Air Pistol Cylinders – Burst Risk (2008)

The recalled Walther air cylinders for air pistols are aluminum and involve model 2/WALTHER 85 cm3, with the imprinted test date between 6 00 and 6 01 2000/2001 located on the end of the cylinder.

CPSCJul 23, 2008Nationwide• Carl Walther GmbH, Sportwaffen, of Germany