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. 2,487 recalls have been distributed to Louisiana in the last 12 months.
Showing 35461–35480 of 51,202 recalls
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: 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 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 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: 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 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: 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: Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 Recalled by...
The Issue: Boost Tea is being recalled for potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...
The Issue: Integra's post QA release review of historical product release test results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...
The Issue: The units have been fitted with a potentially faulty power supply cable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After importing segmentation results of the left atrium created on the Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...
The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...
The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drew Scientific Inc. Drew3-PAC. This D3 Reagent Pack includes: diluent...
The Issue: The reagent pack may result in elevated platelet background during Drew3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HIgH-Flo Subcutaneous Safety Needle Sets Recalled by Repro-Med Systems, Inc....
The Issue: On 2/24/2016 during post sterilization inspection of part number F180...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to If the PDM is...
The Issue: If the PDM is utilized to output a pressure for computing fractional flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.