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. 2,558 recalls have been distributed to Louisiana in the last 12 months.
Showing 19581–19600 of 51,202 recalls
Recalled Item: Class IV New Era medical laser device Recalled by Inova Lasers LLC Due to...
The Issue: The firm failed to comply with the applicable standards regarding Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Electrolyte (2 X 2L) Reagent Recalled by Beckman Coulter Inc. Due to...
The Issue: Electrolyte reagent, used for clinical laboratory testing to determine CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honeywell Pressure Transducer- Part Number: 370506-22. It is a component...
The Issue: The firm is replacing pressure transducers with an improved design due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glycopyrrolate Tabs Recalled by NCS Healthcare of Kentucky Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specification: High Out of Specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tramadol Hydrochloride Tablets USP CIV Recalled by Teva Pharmaceuticals USA...
The Issue: Labeling: Incorrect package insert - Patient leaflets for the specified lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Graviti Pharmaceuticals Private...
The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that one 20 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Southern Sisters Gourmet Cheddar Garlic Biscuits Recalled by Southern...
The Issue: Undeclared allergen: Wheat Undeclared colors: Yellow #5 and #6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Apple Crisp mix Recalled by Southern Sisters...
The Issue: Undeclared allergen: Pecans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Butter Pecan Cheeseball mix Recalled by Southern...
The Issue: Undeclared allergens: Milk, Wheat, Soy, and Almond.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Shrimp and Stone-Ground Grits Recalled by Southern...
The Issue: Undeclared allergen: Milk. Undeclared colors: Yellow #5 and #6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Taco Soup Recalled by Southern Sisters Gourmet Due...
The Issue: Undeclared allergens: Milk and Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Crab Cake Mix Recalled by Southern Sisters Gourmet...
The Issue: Undeclared allergens: Wheat and Soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Oven Fried Chicken Recalled by Southern Sisters...
The Issue: Undeclared allergen: Wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Southern Sisters Gourmet Caramel Apple Cobbler Recalled by Southern Sisters...
The Issue: Undeclared allergen: Wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...
The Issue: The spike rail was manufactured with an oversized thru-hole which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...
The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...
The Issue: An internal component was assembled in the incorrect orientation, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...
The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.