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 32813300 of 52,570 recalls

Medical DeviceJanuary 29, 2025· Pentax of America Inc

Recalled Item: PENTAX Medical Video Colonoscope- Intended to provide optical visualization...

The Issue: During endoscopic procedures using a combination of the video processor...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System (sodium bicarbonate...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Soft Tip NETI POT Nasal Wash System (sodium bicarbonate Recalled...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 28, 2025· Ascent Consumer Products Inc.

Recalled Item: SinuCleanse Premixed SALINE PACKETS (sodium bicarbonate USP 700 mg and...

The Issue: Microbial Contamination of Non-Sterile Products: Bacterial contamination...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Optima XR646 HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Definium 656HD & Discovery XR656HD (GTINs: 00840682138598 Recalled by GE...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656 HD. X-Ray imaging system. Recalled by GE Medical Systems,...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· TAS Medical Inc

Recalled Item: TISSUE APPROXIMATION SYSTEM (TAS) Recalled by TAS Medical Inc Due to Tissue...

The Issue: Tissue approximation straps (zip-ties) have broken before or during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH Recalled...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B0CY2RDW5T Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B084PZ7K98 Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund