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. 2,526 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,526 in last 12 months

Showing 3338133400 of 53,528 recalls

DrugNovember 14, 2016· Akorn Inc

Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...

The Issue: Failed Stability Specifications; out-of specification value for homogeneity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2016· Ultimate Body Tox

Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...

The Issue: Software error due to the filament on timer

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

Class II — Potential Health HazardOngoing
FoodNovember 12, 2016· KRAFT HEINZ FOODS COMPANY

Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...

The Issue: Possible contamination of product with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 11, 2016· House Of Flavors, Inc.

Recalled Item: Ashby's Sterling Peanut Butter Landslide Ice Cream Recalled by House Of...

The Issue: House of Flavors, Inc. is voluntarily recalling a limited portion of Ashby's...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 11, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...

The Issue: Lack of 510k clearance for design modification.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2016· Halyard Health

Recalled Item: Sterling Nitrile Sterile Powder Free Exam Gloves Recalled by Halyard Health...

The Issue: Defects: Product may be discolored and brittle resulting in the inability of...

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

Class II — Potential Health HazardOngoing
FoodNovember 10, 2016· Agave Dream

Recalled Item: Agave Dream Chocolate 1 Pint Code 8 9934900202 4 Recalled by Agave Dream Due...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2016· American Blue Ribbon Holdings DBA Legendary Baking

Recalled Item: Ultimate Chocolate Chip Cookie Dough Pie Recalled by American Blue Ribbon...

The Issue: Product incorporated cookie dough that was potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2016· Agave Dream

Recalled Item: Agave Dream Cappuccino 1 Pint Code 8 9934900204 8 Recalled by Agave Dream...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2016· Agave Dream

Recalled Item: Agave Dream Vanilla 1 Pint Code 8 9934900201 7 Recalled by Agave Dream Due...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2016· Agave Dream

Recalled Item: Agave Dream Chocolate Chip 1 Pint Code 8 9934900302 1 Recalled by Agave...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 10, 2016· Agave Dream

Recalled Item: Agave Dream Lavender 1 Pint Code 8 9934900206 2 Recalled by Agave Dream Due...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 9, 2016· Seth Ellis Chocolatier, LLC

Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...

The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...

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

Class I — Serious Health HazardOngoing
Refund