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. 1,080 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,080 in last 12 months

Showing 12561–12580 of 52,570 recalls

FoodMay 11, 2022· EarthLab Inc

Recalled Item: Wise Woman Herbals Kava Capsules Recalled by EarthLab Inc Due to The...

The Issue: The microbial test result is found to be out of specification due to high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2022· EarthLab Inc

Recalled Item: Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength...

The Issue: The microbial test result is found to be out of specification due to high...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 11, 2022· EarthLab Inc

Recalled Item: Wise Woman Herbals Standardized Kava Glycerite Recalled by EarthLab Inc Due...

The Issue: The microbial test result is found to be out of specification due to high...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% Recalled by Novartis...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2022· AMS Packaging Inc

Recalled Item: Premium Nature Instant Hand Sanitizer Recalled by AMS Packaging Inc Due to...

The Issue: Subpotent Drug: FDA analysis has revealed some bottles of these products...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Xiidra (lifitegrast ophthalmic solution) 5% PROFESSIONAL SAMPLE Recalled by...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Xiidra (lifitegrast ophthalmic solution) Recalled by Novartis...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 10, 2022· GE Healthcare, LLC

Recalled Item: CARESCAPE Central Station (CSCS) V2 Recalled by GE Healthcare, LLC Due to...

The Issue: The CARESAPE Central Station (CSCS) V2 can shut down due to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394600 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock with OFF Directed Tap Without Extension Tube Recalled...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (20 Ga Blue) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS) Recalled by...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta" Plus3 White Blend OEM (sterile Recalled by Becton Dickinson &...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) Recalled by Becton...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2022· Becton Dickinson & Company

Recalled Item: Nexiva with Single BD Connecta Stopcock Version (Pink) Catalog No. 383687...

The Issue: May have the potential for leakage at the housing component of the stopcock,...

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

Class II — Potential Health HazardOngoing