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Recalls distributed in Missouri

These notices name Missouri in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,082 stored notices name Missouri, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Missouri too — those are in the archive.

Medical devices

Reported Sep 23, 2020

NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Novarad Corporation

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2020

Back to Nature, Organic Rosemary and Olive Oil Stoneground Wheat Cracker, 6 oz. foil bag inside paper carton, 6…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B&G Foods North America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2020

BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

CareFusion 303, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2020

Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hellofresh US

FDA (openFDA food enforcement)

Medical devices

Reported Sep 16, 2020

Merge PACS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MicroPort Orthopedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2020

Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 50# A1, Model No.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Talladium Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

BD Alaris System. The EtCO2 module is a capnograph indicated for continuous, noninvasive monitoring of end tidal carbon…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product Number: R30165501, UDI-DI: 05056080501826 -…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Europe Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

Symbia S-Series and Symbia T-Series - Product Usage: Intended use of the device SPECT: To detect or image the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2020

StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ4-RCV-A0 EU - Product Usage: is used…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stimwave Technologies Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 9, 2020

Taylor Farms Foodservice Onion Yellow Dice 1/8" Pack Size 4/5#; Taylor Farms Foodservice Onion Yellow Dice 1/4" Pack…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Farms Texas, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 2, 2020

CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biosense Webster (israel), Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

Flexible Intubation Fiberscope, Part: 11301AA1, with Instruction Manual: Z18441US - Product Usage: are intended to be…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Neurovision Medical Products Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 2, 2020

E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 2, 2020

The following products received from the UNFI Distribution Center Champaign, IL on 7/12/2020: Ditch Farms Eggs brand:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

UNFI General Corporate

FDA (openFDA food enforcement)

Medical devices

Reported Aug 26, 2020

Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 26, 2020

HIGH LINER FOODSERVICE***Genuine Maryland-Style Premium Crab Cakes***48-3 oz***KEEP FROZEN***10004302***PRODUCT OF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

High Liner Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 26, 2020

Earth Grown brand Mocha Fudge Non-Dairy Frozen Dessert in pint sized paperboard carton with a paperboard lid.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Smith Foods Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 26, 2020

MURRAY'S CHADS SMOKED GOUDA DIP in plastic tubs, all sizes.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 19, 2020

HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HF Acquisition Co., LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2020

AVE 2 Birthing Bed - Product Usage: is designated to be used by mothers ready for spontaneous vaginal delivery and also…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Linet Americas

FDA (openFDA device enforcement)

Medical devices

Reported Aug 19, 2020

Verigene Processor SP with assay: Luminex, VERIGENE Gram-Positive Blood Culture Nucleic Acid Test,BC-GP, IVD - Product…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

1 more product in this recall

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.