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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 2621–2640 of 13,412 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: QP COUGH COLD TABLET 16 CT distributed to specific Family 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.
Recalled Item: NPX ENEMA 4.5 FL OZ 2 PK distributed to specific 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.
Recalled Item: MIDOL COMPLETE CAPLET 16 CT SKU 913028 QP MENSTRUAL RELIEF Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMBI NRSHNG DAILY FACIAL MSTURZER 1.7 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.
Recalled Item: DR SCHOLLS CLR AWAY LIQ WART REMVR 20CT SKU 998384 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.
Recalled Item: GUARDIAN ANTACID EX STRGTH TBLT FRT 96CT SKU 901379 GUARDIAN Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 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.
Recalled Item: SWAN CALAMINE LOTION 6 FL 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.
Recalled Item: MIRALAX 8.3 OZ distributed to specific Family Dollar Stores 04/30/2022...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.