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. 1,064 recalls have been distributed to North Carolina in the last 12 months.
Showing 16561–16580 of 29,737 recalls
Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...
The Issue: The manufacturer has discovered that potentially out-of-specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.