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. 2,646 recalls have been distributed to Louisiana in the last 12 months.
Showing 13021–13040 of 51,202 recalls
Recalled Item: Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit Recalled by Wilton...
The Issue: Milk is missing from the product's allergen Contains statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...
The Issue: QC process was not adequate for the specification range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...
The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GONADORELIN (5ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc., dba APS...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable Recalled by Drug...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable Recalled by Drug...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable Recalled by Drug Depot,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed Dissolution Specifications; during long term stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable Recalled...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: (CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc.,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...
The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...
The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...
The Issue: Product not approved for release for US distribution
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...
The Issue: Product was sterilized with a higher than specification EO concentration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.