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. 924 recalls have been distributed to Louisiana in the last 12 months.
Showing 45981–46000 of 51,202 recalls
Recalled Item: The Chobani Flip product come in 5.3oz (150g) square plastic Recalled by...
The Issue: Greek yogurt product Chobani brand is recalled due to report of illnesses...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 6/16 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Pineapple Blended Recalled...
The Issue: Greek yogurt product Chobani brand is recalled due to report of illnesses...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 12/6 oz. Chobani 0% Non-Fat Greek Yogurt Pear Fruit on the Bottom Recalled...
The Issue: Greek yogurt product Chobani brand is recalled due to report of illnesses...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 6/4/3.5 oz. Champions 1.5% Milkfat Low-Fat Greek Yogurt Strawberry Recalled...
The Issue: Greek yogurt product Chobani brand is recalled due to report of illnesses...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate covered wafers (Bocadin) in plastic packaging sold under the...
The Issue: Undeclared Allergens (Milk): Mi Costenita BOCADIN wafer with chocolate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aldactone (spironolactone) tablets Recalled by Pfizer Us Pharmaceutical...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spironolactone tablets Recalled by Greenstone Llc Due to Marketed without an...
The Issue: Marketed without an Approved NDA/ANDA: This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cranial Access (CRAK) Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra is recalling certain lots of Cranial Access Kit due to a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1200 System Software: 1) V2.00 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Recalled by Cincinnati Sub-Zero Products Inc Due to During a...
The Issue: During a label review it was discovered that both the Blanketrol III...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine Recalled by Novartis Consumer Health Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: The products are being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Creafuse Grape Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creafuse Fruit Punch Recalled by GE PHARMA LLC - Due to Product contains 1,3...
The Issue: Product contains 1,3 dimethylamylamine (DMAA)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DANNON OIKOS Fruit on the Bottom GREEK NONFAT YOGURT BLUEBERRY 0% FAT...
The Issue: OIKOS Nonfat Yogurt Blueberry Flavor Single Serve 5.3 oz cups were recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.