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. 1,937 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,937 in last 12 months

Showing 2286122880 of 52,570 recalls

Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 45MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2019· Covidien LLC

Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...

The Issue: The device may be missing one of two pin components that maintain alignment...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...

The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...

The Issue: There is the possibility of viewing studies directly from the Enterprise...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert C. difficile/Epi Control Panel Recalled by Microbiologics Inc...

The Issue: Product is labeled with expiration date of 2021-10-31, should be 2021-03-31.

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

Class III — Low RiskOngoing
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2019· APS BioGroup, Inc

Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...

The Issue: The recall is being conducted as a result of elevated APC levels. Through...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund