All Recalls

95,094 total recalls in our database

The implantable pulse generator (IPG) model 2408 had suboptimal performance establishing a connection to the external devices unless they were brought into close proximity (as close as 5 cm). The following functions may not be available: Reprogramming the stimulator, Adjusting stimulation parameters (on/off, intensity modifications, stimulation program selection), and Recharging the stimulator.

Jan 26, 2016 Implants & Prosthetics View Details →

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

Jan 13, 2016 Diagnostic Equipment Nationwide View Details →

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

Jan 13, 2016 Diagnostic Equipment Nationwide View Details →

The implantable pulse generator (IPG) model 2408 had suboptimal performance establishing a connection to the external devices unless they were brought into close proximity (as close as 5 cm). The following functions may not be available: Reprogramming the stimulator, Adjusting stimulation parameters (on/off, intensity modifications, stimulation program selection), and Recharging the stimulator.

Jan 26, 2016 Other Medical Devices View Details →

Medtronic Navigation is recalling the Biotex Adapter Kit because it was commercially distributed by BioTex without a cleared premarket [510(k)] from FDA.

Feb 22, 2016 Surgical Instruments View Details →

When a user performed radiography using the wireless FPD, a message window appeared on the monitor stating that imaging transmission was not completed with no radiographic image. It also indicated to select the "OK" button to re-acquire the image data or to select the¿'Cancel" button to cancel the re-acquisition. As instructed the user selected "OK" and the same message window appeared. This same operation was repeated several times with the identical result - no image. Finally, the user selected "Cancel" and the re-acquisition was terminated.

Jan 14, 2016 Other Medical Devices Nationwide View Details →

Straight needle labeled as a curved needle

Feb 26, 2013 Surgical Instruments Nationwide View Details →

Cook Medical is voluntarily recalling specific lots of the Ultraxx" Nephrostomy Balloon Set and the Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set because of a labeling mix-up. Cook Medical has received reports of packages labeled as Ultraxx" Nephrostomy Balloon Set actually containing the Ascend¿ AQ¿ Ureteral Dilation Balloon Catheter Set and vice versa.

Jan 27, 2016 Surgical Instruments View Details →

Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream specimen kits are contaminated with bacteria

Jan 22, 2016 Diagnostic Equipment Nationwide View Details →