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. 2,598 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,598 in last 12 months

Showing 1272112740 of 28,172 recalls

Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Advanix Pancreatic Stent Recalled by Boston Scientific Corporation...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Boston Scientific Corporation

Recalled Item: Boston Scientific Advanix Pancreatic Stent Recalled by Boston Scientific...

The Issue: Product manufactured between September 29, 2017 and September 12, 2019 have...

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

Class II — Potential Health HazardOngoing