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 4822148240 of 53,528 recalls

FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Quick Thin (citrus aurantium extract Recalled by Bethel Nutritional...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 5, 2013· Bethel Nutritional Consulting, Inc

Recalled Item: Bethel Advance (bitter orange Recalled by Bethel Nutritional Consulting, Inc...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analyses detected the presence of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario Diagnostic Ultrasound System SSA-660A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Medicel Ag

Recalled Item: Product Name: nanoPOINT Injector System Recalled by Medicel Ag Due to The...

The Issue: The firm initiated this recall of one lot (121402) of nanoPOINT Injectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio MX Diagnostic Ultrasound System SSA-780A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company - Health Care Business

Recalled Item: 3M Scotchcast Recalled by 3M Company - Health Care Business Due to 3M is...

The Issue: 3M is conducting a voluntary product recall of selected lots of 3M"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Aplio XG Diagnostic Ultrasound System SSA-790A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· Toshiba American Medical Systems Inc

Recalled Item: Xario XG Diagnostic Ultrasound System SSA-680A Used for routine diagnostic...

The Issue: The firm initiated this recall of certain Toshiba Diagnostic Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2013· 3M Company/3m Espe Dental Products

Recalled Item: 3M ESPE Unitek Primary Stainless Steel Crowns (First Primary UL4) Recalled...

The Issue: 3M ESPE is recalling Unitek Primary Stainless Steel Crowns (First Primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2013· Villa Radiology Systems LLC

Recalled Item: Juno DRF System. Mobile X-ray system These are general Recalled by Villa...

The Issue: It has been discovered that the Air Kerma rate information is inconsistent...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2013· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ranitidine Hydrochloride Tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Microbial Contamination of Non-Sterile Products: A lot of raw material used...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2013· American Health Packaging

Recalled Item: Valacyclovir HCl Tablets Recalled by American Health Packaging Due to Subpotent

The Issue: Subpotent

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 2, 2013· La Terra Fina USA, Inc.

Recalled Item: Chunky Spinach Artichoke and Parmesan Dip: Gluten Free Recalled by La Terra...

The Issue: One lot Spinach Artichoke & Parmesan dip contains the ingredient and...

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

Class III — Low RiskOngoing
Refund
FoodAugust 1, 2013· Gourmet Express Marketing, Inc.

Recalled Item: Breaded Recalled by Gourmet Express Marketing, Inc. Due to Packages of...

The Issue: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 1, 2013· Superior Nut Co. Inc.

Recalled Item: Raw Pistachio Halves Recalled by Superior Nut Co. Inc. Due to Potential...

The Issue: Positive laboratory result for Salmonella sp. Speciation in progress.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 1, 2013· AbbVie Inc.

Recalled Item: Mavik¿ trandolapril tablets 4mg Recalled by AbbVie Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Package Insert; product packaged with outdated version...

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

Class III — Low RiskOngoing
Refund