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. 2,729 recalls have been distributed to Indiana in the last 12 months.
Showing 7921–7940 of 13,412 recalls
Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...
The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...
The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...
The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...
The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...
The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...
The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...
The Issue: Presence of foreign substance: The recall was initiated due to black...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications: out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules Recalled by DYNAMIC...
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCL in 0.9% Sodium Chloride injectable Recalled by SCA...
The Issue: Lack of assurance of sterility: Product bags leaking at seam.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saphris 10 mg (asenapine) sublingual tablets Recalled by Forest...
The Issue: Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable Recalled by...
The Issue: Lack of assurance of sterility: Product bags leaking at seam.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable Recalled by SCA...
The Issue: Lack of assurance of sterility: Product bags leaking at seam.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable Recalled by...
The Issue: Lack of assurance of sterility: Product bags leaking at seam.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable Recalled by SCA...
The Issue: Lack of assurance of sterility: Product bags leaking at seam.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.