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. 2,609 recalls have been distributed to Louisiana in the last 12 months.
Showing 15601–15620 of 29,201 recalls
Recalled Item: Stryker Mako Vizadisc Knee Procedure Tracking Kit Recalled by Mako Surgical...
The Issue: Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CKMB Calibrator 2-pack Japan Recalled by Siemens Healthcare...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CKMB Master Curve Material Recalled by Siemens Healthcare...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CKMB Calibrator Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CKMB Master Curve Material Recalled by Siemens Healthcare...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Plus Recalled by Diagnostica Stago,...
The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Recalled by Diagnostica Stago, Inc....
The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE...
The Issue: BioFlo Ports was partially manufactured with the incorrect sterile port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom EV0-2 with any version of EVOware and EVOware Sample Recalled by...
The Issue: There is a software issue that can potentially impact sample identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ1 Advanced XL Recalled by Qiagen Sciences LLC Due to An issue with the...
The Issue: An issue with the power branching printed circuit board (PCB) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear Recalled by...
The Issue: Johnson and Johnson Vision Care received a number of reports of a partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Polyisoprene Condoms Recalled by Reckitt Benckiser LLC Due...
The Issue: The products failed the filed specification of 1.0kPa for Burst Pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BULK NONSTERILE PERIFIX CATHETER CONN. Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFSDTD EPID TRAY W/17GA FIXED WING Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CNB200TKU NON-STIM CATH FULL KIT Recalled by B. Braun Medical, Inc. Due to...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TFC CONTINUOUS EPID SET W/17G TUOHY Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CNBFX350O CONTIPLEX CONT NERVE BLOCK Recalled by B. Braun Medical, Inc. Due...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TK ACCU-BLOC PERIFIX KIT Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18H CONT EPIDURAL SET Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ES1725K SPINAL/EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.