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 7641–7660 of 13,412 recalls
Recalled Item: Medline General Purpose Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Incision Drainage Kit Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline GHS Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Straight Suture Removal Tray Recalled by Medline Industries Inc Due...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline Suture Removal Tray Recalled by Medline Industries Inc Due to...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Professional Hospital Supply Suture Removal Kit Recalled by Medline...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liberator Medical Supply Catheter Insertion Tray Recalled by Medline...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline All Purpose Instrument Tray Recalled by Medline Industries Inc Due...
The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinonide Gel USP Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...
The Issue: Cross contamination with other products: traces of Dapsone were found in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Intralipid 20% Recalled by Baxter Healthcare Corporation Due to Temperature...
The Issue: Temperature Abuse: A portion of this product lot was exposed to subfreezing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: grande X 5800 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIFTY SHADES 6000 capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RHINO 7 Platinum 5000 Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PapaZen 3300 capsule Recalled by Gadget Island, Inc Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminocaproic Acid Recalled by Medisca, Inc. Due to CGMP Deviations: Product...
The Issue: CGMP Deviations: Product manufactured for Industrial Use but was labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.