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. 2,828 recalls have been distributed to North Carolina in the last 12 months.
Showing 2041–2060 of 29,737 recalls
Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...
The Issue: In situations where two images with differing Fields of View (FOV) complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Systems Manager Recalled by CareFusion 303, Inc. Due to Software...
The Issue: Software issue that may result in outdated automated programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Care Coordination Engine (CCE) Infusion Adapter Recalled by CareFusion...
The Issue: Software issue that may result in outdated automated programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Coated Super Tampons and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Month Regular Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to Product...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 36 Coated Regular Tampons Recalled by DAYE (ANNE'S DAY LTD) Due...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Coated Super and 9 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 3 Month Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 3 Month All in One Bundle Recalled by DAYE (ANNE'S DAY LTD) Due...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 36 Coated Super Tampons Recalled by DAYE (ANNE'S DAY LTD) Due to...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trial Tampon Box Recalled by DAYE (ANNE'S DAY LTD) Due to Product lacks...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 3 Month Regular Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heavy Flow Bundle Recalled by DAYE (ANNE'S DAY LTD) Due to Product lacks...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Coated Regular and 9 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Super and 18 Nude Super Tampons Recalled by DAYE (ANNE'S DAY LTD)...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.