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. 2,547 recalls have been distributed to Louisiana in the last 12 months.
Showing 20721–20740 of 51,202 recalls
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prasugrel Tablets 5 mg Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Low out of specification dissolution results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...
The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viatrexx-Articula Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Ouch Recalled by 8046255 Canada Inc. DBA Viatrexx Due to Lack of...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viatrexx-Connectissue Recalled by 8046255 Canada Inc. DBA Viatrexx Due to...
The Issue: Lack of Assurance of Sterility: products manufactured in a manner than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.