Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,038 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,038 in last 12 months

Showing 20881–20900 of 52,570 recalls

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· 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· 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· Haemonetics Corporation

Recalled Item: JAPAN DISP SET Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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