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. 2,506 recalls have been distributed to Louisiana in the last 12 months.
Showing 31241–31260 of 51,202 recalls
Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...
The Issue: Product was tested and found positive for Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's All Natural Unsweetened Apple Sauce Recalled by Manzana...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Organic Unsweetened Apple Sauce Recalled by Manzana Products...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joes Imported English Authentic Lemon Curd Recalled by Trader Joes...
The Issue: Trader Joe's Co. is recalling the Lemon Curd because it contains undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce Recalled by...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BrightView XCT model number 882482 BrightView and BrightView X are Recalled...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT model number 882480 BrightView and BrightView X are...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...
The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X 3/4 model number 882479 BrightView and BrightView X Recalled by...
The Issue: The brake hub was not engaging with the gear box shaft due to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penicillin V Potassium Tablets Recalled by Citron Pharma Llc Due to Presence...
The Issue: Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aspirin Chewable Tablets Recalled by Mckesson Packaging Services Due to...
The Issue: Presence of Foreign Substance: foreign material found in the bulk inventory.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...
The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...
The Issue: The bed exit alarm may not function properly if the alarm has been armed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...
The Issue: The integrity of the sterile packaging is potentially compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems...
The Issue: Philips identified a 4D CT pulmonary phase issue on Brilliance BigBore...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.