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 13021–13040 of 52,570 recalls

Medical DeviceApril 11, 2022· TELEFLEX MEDICAL INC

Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...

The Issue: Reports received of torn corrugated breathing tubes.

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

Class II — Potential Health HazardOngoing
DrugApril 11, 2022· Torrent Pharma Inc

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Torrent Pharma Inc...

The Issue: CGMP deviations: tablets cracking

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 8, 2022· Microtek Medical Inc.

Recalled Item: TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content...

The Issue: Latex content in product was labeled incorrectly as latex free.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Radiometer Medical ApS

Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...

The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Instrumentation Laboratory

Recalled Item: HemosIL ReadiPlasTin Recalled by Instrumentation Laboratory Due to Variable...

The Issue: Variable and out of specification QC results with HemosIL ReadiPlasTin. IL...

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

Class II — Potential Health HazardOngoing
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Sugar-Free Xylitol NET 8.45 FL OZ Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Honey Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Rock Sugar Flavor NET 4.45 FL Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Coconut Flavor NET 8.45 FL OZ Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 7, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: Resin UPDATE CD-ROM Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The problem is with the Bio-Rad VARIANT nbs Sickle Cell Program Resin Update...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· MALVERN PANALYTICAL LTD

Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...

The Issue: Product found to not comply to Class 1 Laser safety requirement.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· Synthes (USA) Products LLC

Recalled Item: Radial Head Replacement System Implant is a one-piece Recalled by Synthes...

The Issue: DePuy Synthes Radial Head Replacement System Contraindications added to...

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

Class II — Potential Health HazardOngoing
DrugApril 7, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Rifampin for Injection Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 6, 2022· Johnson & Johnson Surgical Vision Inc

Recalled Item: TRAY RING COVER Recalled by Johnson & Johnson Surgical Vision Inc Due to...

The Issue: Potential breach in the sterility barrier for tray ring covers.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2022· MESA BIOTECH, INC

Recalled Item: Accula SARS-CoV-2 Test Recalled by MESA BIOTECH, INC Due to SARS-CoV-2 Test...

The Issue: SARS-CoV-2 Test has an increased potential for false positive results, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 6, 2022· Helena Laboratories, Corp.

Recalled Item: V8 Immunodisplacement Kit Recalled by Helena Laboratories, Corp. Due to Due...

The Issue: Due to microbial growth causing interference with interpretation.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2022· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Sara Plus Active Floor Lift Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due...

The Issue: The device may emit smoke or ignite.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 5, 2022· Certified Safety Mfg Inc

Recalled Item: The following first aid kits and cabinets containing components Medi-First...

The Issue: First aid kit and cabinet components are being recalled by the supplier due...

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

Class II — Potential Health HazardOngoing