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. 2,711 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,711 in last 12 months

Showing 561580 of 52,570 recalls

FoodDecember 3, 2025· McCain Foods USA Inc

Recalled Item: Ore-Ida Tater Tots shaped potatoes Recalled by McCain Foods USA Inc Due to...

The Issue: Clear hard plastic fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148 Recalled by Philips...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T. Product Code (REF): (1) 781342 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Medtronic Neuromodulation

Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...

The Issue: Complaints received that Vanta A71200 CP App does not function as intended...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Boston Scientific Corporation

Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...

The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 Recalled by CareFusion...

The Issue: Due a software issue that may result in equipment not receiving timely...

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2025· Fazt & Loud LLC

Recalled Item: Lost and Found Energy Recalled by Fazt & Loud LLC Due to Recall is due to a...

The Issue: Recall is due to a misprint on the label that incorrectly identifies the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing