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. 2,137 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,137 in last 12 months

Showing 16811700 of 52,570 recalls

Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Philips Medical Systems Nederland B.V.

Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...

The Issue: Software issue that results in the display of outdated information.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Theophylline extended-release tablets 400mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Failure results (above) were reported for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2025· Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...

The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...

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

Class III — Low RiskOngoing
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2025· Cepheid

Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...

The Issue: As a result of Post-Market half-time stability testing, false negative test...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000....

The Issue: Reports of out-of-box failures discovered during the limited launch phase....

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

Class II — Potential Health HazardOngoing
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH...

The Issue: Unapproved Drug Claims and Misbranded.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild...

The Issue: Unapproved Drug Claims.

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2025· Hi-Tech Pharmaceuticals Inc.

Recalled Item: LGSCIENCES BATTLE HARDENER PLATINUM SERIES COMPLETE 6 WEEK CYCLE WITH...

The Issue: Unapproved Drug Claims.

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

Class III — Low RiskOngoing
Refund