💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
All Recalls
95,038 total recalls in our database
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Regular Strength Zantac 150 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 67751-151-01.
Sanofi-Aventis U.S.
💊 Drugs Class I - Dangerous
CGMP Deviations: Presence of NDMA impurity detected in product.
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
💊 Drugs Class I - Dangerous
CGMP Deviations: Presence of NDMA impurity detected in product.
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Regular Strength Zantac 150 mg Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 05269-220-25.
Sanofi-Aventis U.S.
💊 Drugs Class I - Dangerous
CGMP Deviations: Presence of NDMA impurity detected in product.
💊 Drugs Class I - Dangerous
Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules
Synchromed II programmable pump, Model numbers 8637-20 and 8637-40
Medtronic Neuromodulation
🏥 Medical Devices Class I - Dangerous
There is a potential for the presence of a foreign particle inside the pump motor assembly which could interfere with the motor gear rotation and lead to a permanent motor stall.
🏥 Medical Devices Class I - Dangerous
Potential for the Quantum 2000 Electrosurgery Generator, part numbers 909075, 909075-05 and 909075-05W, to cease to either cut, coagulate, or blend during a procedure when the foot pedal is used for activation.
Quantam 2000 Electrosurgical Generator, Part number 909075.
CooperSurgical
🏥 Medical Devices Class I - Dangerous
Potential for the Quantum 2000 Electrosurgery Generator, part numbers 909075, 909075-05 and 909075-05W, to cease to either cut, coagulate, or blend during a procedure when the foot pedal is used for activation.
🏥 Medical Devices Class I - Dangerous
Device was shipped without a Unique Device Identification (UDI) label.
🏥 Medical Devices Class I - Dangerous
There is a potential for the cuff to leak air leading to a loss of vascular occlusion.
🏥 Medical Devices Class I - Dangerous
Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.
🏥 Medical Devices Class I - Dangerous
There is a potential for the cuff to leak air leading to a loss of vascular occlusion.
🏥 Medical Devices Class I - Dangerous
The locking pin of the front wheel asse mbly of the Evolution Transfer Carriages may not remain full y engaged with the transfer carriage and result in the transfer carriage and loading car unexpectedly falling forward