Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,988 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3001–3020 of 47,654 recalls
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: 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 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: Aveir DR Leadless Pacemaker (LP) Ventricular Device UDI-DI Recalled by...
The Issue: Due to a manufacturing issue, leadless pacemakers may have been exposed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ulker Rulokat Hazelnut Wafers Recalled by ZB Importing LLC Due to Undeclared Egg
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ulker Biskrem Cocoa Biscuit Recalled by ZB Importing LLC Due to Undeclared Wheat
The Issue: Undeclared wheat and egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ulker Dankek Roll Cake Banana Recalled by ZB Importing LLC Due to Wheat not...
The Issue: Wheat not listed in Contains statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ulker Kekstra Mini strawberry Recalled by ZB Importing LLC Due to Milk not...
The Issue: Milk not declared as the major food allergen source for the ingredient Whey
Recommended Action: Do not consume. Return to store for a refund or discard.