All Recalls

95,075 total recalls in our database

Marketed Without An Approved NDA/ANDA: This product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was withdrawn from the U.S. market in October 2010 due to safety concerns, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.

Feb 14, 2018 Prescription Drugs View Details →

Medtronic implemented a final design change intended to address the motor stall due to corrosion and is recalling devices with the previous design that are not implanted.

Aug 9, 2017 Implants & Prosthetics Nationwide View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

23 Software related issues for the IQon Spectral CT with 4.7.2 software version. These issues include: " Software errors that may result in CT spectral images misrepresentation or incorrect treatment; " Software errors that may result in partial set of images or inability to generate CT images.

Jan 11, 2018 Other Medical Devices View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →

INFX-8000C Fluoroscopic X-Ray Systems

Toshiba American Medical Systems

🏥 Medical Devices Class I - Dangerous

During an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the ceiling drive loosened cause the error.

Dec 29, 2017 Other Medical Devices View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →

Range for the same energy could be different depending if the layer is the first layer of the irradiation plan or not.

Oct 19, 2017 Infusion Pumps View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Infusion Pumps Nationwide View Details →