Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,573 recalls have been distributed to North Dakota in the last 12 months.
Showing 2021–2040 of 27,512 recalls
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.
Recalled Item: 3 Month Heavy 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: 36 Coated Super 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 3 Month Heavy 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: 18 Coated Super 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: Regular 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: 36 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: 3 Month Trial Tampon Box 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 18 Coated Super and 18 Nude 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: All in One 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 Coated 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: 9 Coated Regular Tampons and 9 Nude Regular Tampons Recalled by DAYE (ANNE'S...
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 Coated 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: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microstream Instructions for Use and Part Number used with - Product...
The Issue: Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.