All Recalls

95,094 total recalls in our database

The drug fulvestrant (FaslodexΒΏ) may cause falsely elevated estradiol results.

Jan 13, 2016 Diagnostic Equipment Nationwide View Details β†’

Ambu, Aura Gain laryngeal Mask, was found to have lack of Sterility Assurance. The firm discovered the problem during final quality control at manufacturing site. Damage to the sterile barrier (the pouch) may compromise a medical device's sterility,leading to contamination of the product and,ultimately,patient complications.

Feb 10, 2016 Infusion Pumps View Details β†’

Due to a false triggering or detection of the lifting gripper READY signal, sample tubes are not correctly placed back in the Rack Tube Transport (RTT) after the decapping process. Therefore, open sample tubes can be dropped in the cobas p 512, spilling the sample material.

Feb 23, 2016 Other Medical Devices View Details β†’

After importing, the segmentation results appear mirrored at the CARTO system and can't be used for the ablation procedure.

Feb 24, 2016 Diagnostic Equipment Nationwide View Details β†’

Due to Operator Console software anomaly, a change in treatment completion status of the last patient of the day may be altered from "Completed (or Discontinued)" to "Untreated" under specific conditions.

Dec 15, 2015 Other Medical Devices View Details β†’

Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the InstinctΒΏ JavaΒΏ System (IFU reference: 046WAN0000T) and Universal ClampΒΏ System (IFU reference: SNA027-N-90001).

Feb 12, 2016 Infusion Pumps Nationwide View Details β†’

Devices reported to have a smooth texture to the outer surface of the metal, which differed from a previous that had a textured outer surface.

Dec 17, 2015 Implants & Prosthetics Nationwide View Details β†’