All Recalls

95,075 total recalls in our database

Superpotent Drug: Subpotent Drug. FDA analysis found this product to be Out of Specification for assay which could result in either Subpotent and/or Superpotent tablets.

Sep 5, 2017 Prescription Drugs View Details β†’

There have been reported incidents of fluid leaks at the luer connection. Leaks have been confirmed to originate from, or near, the reservoirs clearcolored female luer connecter.

Sep 27, 2017 Infusion Pumps Nationwide View Details β†’

Arthrex part number AR-501-UFLC, size 3, batch 10123297, has the incorrect part number AR-501 ΒΏUFRA, size 1 printed on the patient label inside the box.

Oct 3, 2017 Implants & Prosthetics View Details β†’

Observed instability of the device.

Feb 5, 2013 Diagnostic Equipment Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

The Broad Quantification option of the Symbia product software version VB20A may not allow modification of two data input values. The failure occurs when the system with the Broad Quantification option is calibrated with phantoms that do not have a volume of 6500ml and/or when residual dose needs to be entered.

Nov 7, 2017 Diagnostic Equipment View Details β†’