Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,972 recalls have been distributed to North Carolina in the last 12 months.
Showing 15801–15820 of 29,737 recalls
Recalled Item: AMSCO V-PRO 1 Recalled by Steris Corporation Due to There is the potential...
The Issue: There is the potential for a scenario where a punctured cup of sterilant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Li-ion battery packs used in BIS Vista and BIS View Recalled by Covidien LLC...
The Issue: Revised replacement instructions for the Li-ion battery packs used in BIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Binding Site Human IgM Kit (for SPAPLUS) Recalled by The Binding Site Group,...
The Issue: After running the calibration curve, the recovery of the IgM kit control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR1000 Pivot Rehab Bed AC powered adjustable bed. Recalled by Med-Mizer,...
The Issue: Under certain conditions, when pivoting bed to the extreme left there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YUKON Polyaxial Screws (3.5 X 12 mm Recalled by K2M, Inc Due to Screws had a...
The Issue: Screws had a manufacturing error that could prevent the screw from mating...
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: ADVIA Centaur CKMB Calibrator Recalled by Siemens Healthcare Diagnostics,...
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: 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: 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: 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: 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: 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: 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: Stryker Mako Vizadisc Hip 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: 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: 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: 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: 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: 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.