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 25401–25420 of 29,201 recalls
Recalled Item: SHAPE ARM Recalled by Stryker Communications Due to During the use of the...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...
The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...
The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Universal Cannula Recalled by Teleflex Medical Due...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...
The Issue: Product does not meet minimum needle attachment strength requirements; thus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port Recalled...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm)...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Universal Cannula Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.