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. 2,177 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,177 in last 12 months

Showing 26212640 of 13,412 recalls

DrugJune 28, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...

The Issue: Cross Contamination With Other Products: Product is cross contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2022· Loud Muscle Science

Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...

The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2022· Noven Pharmaceuticals Inc

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Customer complaints received for ripping patches...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 24, 2022· Vi-Jon, LLC

Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: GOOD SENSE OMEPRAZOLE TABLET 14CT SKU 900055 PRILOSEC OTC TABLET Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: VASELINE ECZEMA CALMING THERPY CRM 6.8 OZ distributed to specific Recalled...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: MYLICON INFANT GAS DROPS 0.5 OZ distributed to specific Family Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: CLARITIN ALLERGY LIQ CHLDRNS GRAPE 2 FLOZ SKU 900834 CLARITIN Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: ALEVE ANALGESIC BACK MUSCLE 24 CT SKU 999787 ALEVE PM Recalled by Family...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: FS CLOTRIMAZOLE ANTI FUNGAL CREAM .5 OZ distributed to specific Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU Recalled by Family Dollar...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: AFRIN NO DRIP SEVERE CONGESTION 0.5FL OZ distributed to specific Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: VOLTAREN ARTHRITIS PAIN GEL 20G distributed to specific Family Dollar...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2022· Family Dollar Stores, Llc.

Recalled Item: ORAJEL NON MED TEETHING GEL 0.125 OZ distributed to specific Recalled by...

The Issue: CGMP Deviations: product held outside appropriate storage temperature...

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

Class II — Potential Health HazardOngoing
Refund