Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,661 recalls have been distributed to Mississippi in the last 12 months.
Showing 3121–3140 of 28,172 recalls
Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software...
The Issue: Identified an issue with Selenia Dimensions 1.12.0 and 3Dimensions 2.3.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...
The Issue: Due to convenience kits containing a kit component that is under a recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems Recalled by Siemens...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Maple 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper 1.0 Recalled by Siemens Medical Solutions USA, Inc. Due to If...
The Issue: If ultrasound systems with software, are changed from factory default to :...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS Recalled by Roche...
The Issue: Creatine Kinase (CK) Assay Abnormal calibrations on the cobas¿ c 311/501/502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to Recalled by B Braun...
The Issue: Incomplete insertion of the patient connector of the Streamline Airless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...
The Issue: Due to affected devices that may have bent female IUI connector and may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.