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. 1,781 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,781 in last 12 months

Showing 4646146480 of 53,528 recalls

FoodNovember 16, 2013· Lewis Bakeries-Evansville

Recalled Item: White bread packaged under the following names and sizes: Name Recalled by...

The Issue: The firm found two small food-grade stainless steel fragments in two slices...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 16, 2013· Lewis Bakeries-Evansville

Recalled Item: Whole Grain White Bread packaged under the following names and Recalled by...

The Issue: The firm found two small food-grade stainless steel fragments in two slices...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2013· Physique Enhancing Science

Recalled Item: Physique Enhancing Science ALPHAMINE Recalled by Physique Enhancing Science...

The Issue: Products contain "Aegeline" an unapproved New Dietary Ingredient.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2013· Physique Enhancing Science

Recalled Item: Physique Enhancing Science ENHANCED Recalled by Physique Enhancing Science...

The Issue: Products contain "Aegeline" an unapproved New Dietary Ingredient.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 15, 2013· Intuitive Surgical, Inc.

Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...

The Issue: Firm has become aware of the potential for detachment of the jaw insert for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Shimadzu Medical Systems

Recalled Item: Mobile X-ray System Recalled by Shimadzu Medical Systems Due to Shimadzu...

The Issue: Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 Recalled by...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Intuitive Surgical, Inc.

Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...

The Issue: Firm has become aware of the potential for detachment of the jaw insert for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...

The Issue: During clinical operation, a malfunction may occur causing a system display...

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

Class II — Potential Health HazardOngoing
DrugNovember 15, 2013· Actavis Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablet (XL) 150mg Recalled by...

The Issue: Failed Dissolution Specifications: Failed stability testing for dissolution...

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

Class III — Low RiskOngoing
Refund
DrugNovember 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Fluconazole Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Stability Specifications: this product is below specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 14, 2013· Smith & Nephew Inc.

Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...

The Issue: Modification of the bacterial overflow guard (filter) and related changes to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2013· Smith & Nephew Inc.

Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...

The Issue: Modification of the bacterial overflow guard (filter) and related changes to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2013· Accumetrics Inc

Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...

The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...

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

Class II — Potential Health HazardOngoing
FoodNovember 14, 2013· Crunch Pak, LLC

Recalled Item: Crunch Pak Natural Blue Raspberry Flavor Sliced Apples Recalled by Crunch...

The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 14, 2013· Crunch Pak, LLC

Recalled Item: Crunch Pak Apple Slices with Low Fat Caramel Dip Recalled by Crunch Pak, LLC...

The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 14, 2013· Crunch Pak, LLC

Recalled Item: Crunch Pak Honeycrisp Apple Slices Recalled by Crunch Pak, LLC Due to...

The Issue: Crunch Pak Apple Slices are recalled due to a potential contamination with...

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

Class I — Serious Health HazardOngoing
Refund