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. 1,021 recalls have been distributed to Louisiana in the last 12 months.
Showing 22441–22460 of 51,202 recalls
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811910...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229034A Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model:...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229035A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A...
The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...
The Issue: Packaged dental implant healing abutments were found to contain the wrong...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 8 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 6 Fr 1.5 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SELECTSILICONE" 100% SILICONE FOLEY CATHETER 2-WAY 10 Fr 3 ml Recalled by...
The Issue: Loose silicone particulate was found to be present on the shaft of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Trochar Tip Recalled by Zimmer Biomet, Inc. Due to There is a...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.All (Model #11061630) Recalled by Siemens Medical Solutions USA,...
The Issue: The potential sporadic performance problems may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DVR Crosslock ePAK Depth Gauge Recalled by Zimmer Biomet, Inc. Due to There...
The Issue: There is a potential for weak seals of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfur Colloid Reaction Vial 1.0 mL Recalled by Synthetopes Inc Due to Lack...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-d Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Mertiatide Kit Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-Tetrofosmin Kit 5.0 mL Recalled by Synthetopes Inc Due to Lack of...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-DMSA solution Recalled by Synthetopes Inc Due to Lack of Processing Controls.
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sn-DTPA Kit 10 mg Recalled by Synthetopes Inc Due to Lack of Processing...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.