Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,507 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,507 in last 12 months

Showing 3684136860 of 53,528 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· 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
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· 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
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
FoodJanuary 27, 2016· House Of Flavors, Inc.

Recalled Item: Purple Cow Limited Edition Cookie Butter Ice Cream Recalled by House Of...

The Issue: House of Flavors, Inc. is voluntarily recalling a small batch of 8 oz. cups...

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
Medical DeviceJanuary 26, 2016· Applied Medical Technology Inc

Recalled Item: AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm...

The Issue: The firm received complaints that the product is shorter in length than...

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

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

Recalled Item: Covidien Dover P400 PREM UM 16FR SILV TMP 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 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 CATCH KIT SOAP Item Code: 5205 Castile soap Recalled by...

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 PRECSION PRM 14FR SIL 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