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. 1,827 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,827 in last 12 months

Showing 3640136420 of 52,570 recalls

DrugJanuary 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

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

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Bonita Pharmaceuticals, LLC

Recalled Item: Menthocin Patch with Lidocaine-Strong (Menthol 5% Recalled by Bonita...

The Issue: Marketed without an approved NDA/ANDA

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 80 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 10 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 40 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2016· Golden State Medical Supply Inc.

Recalled Item: Atorvastatin Calcium 20 mg Recalled by Golden State Medical Supply Inc. Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodJanuary 27, 2016· Figi's, Inc

Recalled Item: Figi's Classic Marzipan Recalled by Figi's, Inc Due to Figi's Companies is...

The Issue: Figi's Companies is recalling 8 ounce packages of "Classic Marzipan" because...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2016· Physio-Control, Inc.

Recalled Item: LIFEPAK15 monitor/defibrillator with End-Tidal C02 (EtC02) feature...

The Issue: The firm became aware that when using EtC02 in the kPa or % setting and in a...

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

Class II — Potential Health HazardOngoing
DrugJanuary 26, 2016· Amerisource Health Services

Recalled Item: Candesartan Cilexetil Tablets Recalled by Amerisource Health Services Due to...

The Issue: Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 26, 2016· Apotex Scientific, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...

The Issue: Failed Dissolution Specification: Out of specification dissolution results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 25, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS)...

The Issue: Siemens' conducting a recall due to a potential issue when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FMC7 FITC: Model 430918. FMC7 is intended for in Recalled by Becton,...

The Issue: Becton, Dickinson and Company (BD) has determined that the FMC7 FITC (ASR)...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREM 16FR UL LTX FOLEY TRY CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Accuray Incorporated

Recalled Item: CyberKnife Robotic Recalled by Accuray Incorporated Due to The gun box...

The Issue: The gun box mounting bracket may fail to support the weight of the gun box...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 16FR TMP SNS CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PREM U/M 14FR TMP SNS CSD Item Code: Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover P400 PREM U/M 16FR SLVR FLY Item Code: Recalled by Covidien...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2016· Covidien LLC

Recalled Item: Covidien Dover PPREM 18FR UL LTX FOLEY TRY CSD Item Recalled by Covidien LLC...

The Issue: Aplicare Castile Soap towelettes included in the Foley Trays and Mid stream...

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

Class II — Potential Health HazardOngoing