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. 2,617 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,617 in last 12 months

Showing 1126111280 of 28,172 recalls

Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 34cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE SPECIALIZED ORTHOPEDICS Recalled by Nuvasive Specialized...

The Issue: During explantation, standard removal tools can generate sufficient forces...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Ra Medical Systems, Inc.

Recalled Item: DABRA RA-308 Excimer Laser Recalled by Ra Medical Systems, Inc. Due to Due...

The Issue: Due to the taller wheel mounting on the laser, the laser may fall over...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Sensitivity Troponin I (TNIH) Flex reagent...

The Issue: Dimension Vista High Sensitivity Troponin I (TNIH) may exhibit a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM Recalled...

The Issue: The connector linking the EtCO2 module to the HemoBox may break and become...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2020· Intrinsic Therapeutics, Inc.

Recalled Item: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The...

The Issue: The catalog ( REF ) number on the peelable inner labels (patient sticker)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2020· Remel Europe Ltd.

Recalled Item: Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product...

The Issue: Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2020· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 Software Version R1.0 and R1.1 Recalled by Philips Medical...

The Issue: Philips has become aware of a software issue, where the kV and mA values are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2020· Smith & Nephew Orthopaedics AG

Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...

The Issue: Multiple lots being recalled due to a product design issue

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...

The Issue: Disposable face masks labeled as non-medical were distributed to customers...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...

The Issue: The electrode insulating material on the Cobra EMG ET tube used for...

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

Class II — Potential Health HazardOngoing