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 26941–26960 of 51,202 recalls
Recalled Item: Sodium Chloride 3% Inh. 4 mL NEP #30 NDC 00487-9003-60 30 days supply....
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OPDIVO 40 mg/4 mL SDV NDC 00003-3772-11 28 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sutent 37.5 mg capsules x28 NDC 00069-0830-38 28 days supply Recalled by...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Botox 100 Units Vial NDC 00023-1145-01 90 days supply. Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pulmozyme 1 mg/mL Inh. Soln. #30 NDC 50242-0100-40 30 days supply. Recalled...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 28 days supply Recalled by...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Otezla 30 mg tablet NDC 59572-0631-06 30 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Altera Handset NDC 83490-0678-05 56 days supply Recalled by Kroger Specialty...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACURE Recalled by Diamond Wipes International, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WipeEssentials Wet Wipes (benzalkonium chloride 0.13%) Recalled by Diamond...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...
The Issue: The connector of the power supply was capable of fitting other components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...
The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...
The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Surgical Suite Option Product The MR Surgical Option when Recalled by GE...
The Issue: There is a potential safety issue with the table transfer release of the MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amantadine HCl Capsules Recalled by AVKARE Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: funky chunky Chocolate Pretzels. Pretzels Recalled by Funky Chunky LLC Due...
The Issue: Chocolate Pretzels are being recalled because the pecan pieces may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.