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. 2,558 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,558 in last 12 months

Showing 1620116220 of 49,744 recalls

Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: Product Label - ACUSON Sequoia *** Power Input: 100-240V~ Recalled by...

The Issue: The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack CP 1/4-1/4 Pediatric Set 1/B (PERFUSION M484901D...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK HY10J00R6 ECC SMALL CAR). The Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Perfusion Pack (CUSTOM PACK HY11B40R1 1/4 RESPIRATO). The...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...

The Issue: Products being recalled due to potentially elevated level of bacterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· LumiraDx

Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...

The Issue: Two lots of test strips failed QC testing using blank buffer due to false...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...

The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 3, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....

The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2021· Apotex Corp.

Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...

The Issue: Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund