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. 2,704 recalls have been distributed to Indiana in the last 12 months.
Showing 11381–11400 of 53,528 recalls
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Earth Grown Vegan Garlic & Herb Falafel NET WT 12 OZ (340g) Recalled by...
The Issue: Possible presence of Shiga toxin-producing E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earth Grown Vegan Traditional Falafel NET WT 12 OZ (340g) Recalled by...
The Issue: Possible presence of Shiga toxin-producing E. coli.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril and Hydrochlorothiazide Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate Recalled by Fresenius Medical Care...
The Issue: The "Nominal Chemical Composition" section of the label incorrectly lists...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...
The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Subpotent Drug: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...
The Issue: Out of specification for related substances (impurities).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthopedic blade Recalled...
The Issue: Incorrect configuration of the blades in the package. The blades curve to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.