Product Recalls in Louisiana
Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Louisiana in the last 12 months.
Showing 9201–9220 of 13,548 recalls
Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Ophthalmic Solution (0.3% as base) Recalled by Actavis Pharma...
The Issue: Failed Impurities/Degradation Specifications: Firm voluntarily recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quelicin (Succinylcholine Chloride) Injection Recalled by Hospira Inc. Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 3 (Papaverine 20 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Superpotent Drug: one ingredient was found to be above assay specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 1 (Papaverine 1.8 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 4 (Papaverine 18 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 0 (PGE 20 mcg/mL) Injection Recalled by Meditech Laboratories, Inc...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 2 (Papaverine 9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Stability Does Not Support Expiry: manufactured with an active ingredient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Tablets USP Recalled by Impax Laboratories, Inc....
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 9 (Papaverine 0.9 mg Recalled by Meditech Laboratories, Inc Due to...
The Issue: Lack of Assurance of Sterility: incomplete or missing data regarding production.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SODIUM IODIDE I 131 CAPSULE Recalled by Jubilant Draximage Inc Due to...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...
The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amikacin Sulfate injection USP Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: particulate matter identified as glass in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.