All Recalls

95,114 total recalls in our database

Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate due to the set screw component potentially becoming dislodged from the plate assembly.

Mar 9, 2011 Implants & Prosthetics Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details โ†’

Contact failure in F1 and F4 fuse holders was detected on the EC-5000 CXIII Excimer Laser Corneal Surgery System that could cause a serious adverse event for the patient.

Aug 6, 2012 Infusion Pumps View Details โ†’
๐Ÿฅ Medical Devices Class I - Dangerous

Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Apr 24, 2014 Other Medical Devices Nationwide View Details โ†’

Utility vehicle doors

LSI Products Inc.

๐Ÿ  Consumer Products Class III - Low Risk

The latch pin can disengage from the latch and allow the door to open while the vehicle is moving, posing a risk of ejection of an unrestrained rider and impact or laceration hazards.

Nov 25, 2014 Clothing & Accessories Nationwide View Details โ†’

Bob-Cat Zero Turn Riding Mower

Schiller Grounds Care, Inc., of Johnson Creek, Wisc.

๐Ÿ  Consumer Products Class II - Moderate

The steering control arm component can break under normal use, causing driver to lose control and crash.

Nov 20, 2014 Furniture Nationwide View Details โ†’

Simplex 4100ES Fire Alarm Control Panel

Tyco International de Mexico, S. de R.L. de C.V.

๐Ÿ  Consumer Products Class II - Moderate

A defective chip in the alarm panel can cause premature battery failure and prevent activation of devices during alarm conditions, posing a risk of injury and property damage.

Nov 20, 2014 Furniture Nationwide View Details โ†’

Mondelez Global LLC is conducting a voluntary recall of Chiclets Chewing Gum due to undeclared soy lecithin on the label.

Aug 27, 2014 Other Foods Nationwide View Details โ†’