All Recalls

95,102 total recalls in our database

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Certain lots of the Application Instrument for Sternal ZIPFIX that were previously recalled on August 19, 2015 and subsequently repaired and returned to customers between August 26, 2015 and September 23, 2015. The screws on the repaired instruments have the potential to break or loosen. DePuy Synthes is requesting the return of the repaired device in exchange for a new device.

Oct 19, 2015 Surgical Instruments View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Drive shaft and over speed arm may simultaneously fail potentially resulting in a patient falling during use

Sep 8, 2015 Other Medical Devices Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Sterility of the product cannot be assured.

Oct 21, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

Six (6) PCA 10 Degree Hooded Acetabular Insert-Duration 22 mm (ID) have been distributed in the US, although the 22 mm size was inadvertently omitted from 510(k) #K963612.

Oct 15, 2015 Implants & Prosthetics View Details →

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

Oct 20, 2015 Diagnostic Equipment Nationwide View Details →

During a review of the IFU of the SilverStat Pads, it was found that the IFU did not match that submitted in the original 510k

Oct 14, 2015 Surgical Instruments View Details →

These lots of Oxygen Dial Regulators could have the settings label off by one position. When the indicator arrow points to OFF position, the regulator is actually on the half liter setting (0.50), for the 15 liter. For the 8 liter, instead of being in the OFF position, the regulator will be in the quarter liter setting (0.25).

Oct 8, 2015 Other Medical Devices Nationwide View Details →