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. 1,038 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,038 in last 12 months

Showing 21901–21920 of 52,570 recalls

DrugJuly 19, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...

The Issue: Lack of Assurance of Sterility: Bags have potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...

The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 18, 2019· Medical Intelligence Medizintechnik Gmbh

Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...

The Issue: Sometimes, although the HexaPOD has reached the target position, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Arrow International Inc

Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...

The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas e 601 module (cobas 6000 Modular Series system) Part Number:...

The Issue: Quality issue with high pressure solenoid valves may cause inaccurate results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c513 Analyzer Recalled by Roche Diagnostics Operations, Inc. Due to...

The Issue: Quality issue with high pressure solenoid valves

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas 8000 Modular Analyzer Series: cobas 8000 ISE module part Recalled by...

The Issue: Quality issue with high pressure solenoid valves

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

Class II — Potential Health HazardOngoing
FoodJuly 18, 2019· National Frozen Foods Corporation

Recalled Item: Great Value Chopped Spinach Recalled by National Frozen Foods Corporation...

The Issue: Spinach was recalled due to a potential for contamination with Listeria...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2019· Mountain Rose Inc. dba Mountain Rose Herbs

Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...

The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA XT Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK TNA 2 Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max StaphSR Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Vaginal Panel Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 2 USA Recalled by Becton Dickinson & Co. Due to The foil...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing