D-1450-2022 Class II Ongoing
FDA drug recall D-1450-2022 was initiated by Family Dollar Stores, Llc. on Jun 23, 2022 and is designated Class II. Reason for recall: CGMP Deviations: product held outside appropriate storage temperature conditions. The recall status is ongoing.
Recall Details
- Product Type
- Drugs
- Report Date
- Aug 31, 2022
- Initiation Date
- Jun 23, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
QP DPHNHDRME ALRGY MIN TBLT 12 CT SKU 900449 QP ALLERGY DIPHENHYDRAMINE 25 MG 48 CT SKU 916003 QP ALLERGY MULTI SYMPTOM CAPLET 24CT SKU 916918 BENADRYL D CHILD ALLERGY SINUS GRAPE 4FO SKU 901738 GOOD SENSE CHILD ALLERGY CHERRY 4 FL OZ SKU 916917 BENADRYL ALLERGY CONGESTN ULTRA TAB 24CT SKU 999834 BENADRYL ALLERGY ULTRATAB 24CT SKU 902217 BENADRYL ALLERGY LIQUIDGELS 24 CT SKU 916715 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Reason for Recall
CGMP Deviations: product held outside appropriate storage temperature conditions.
Distribution Pattern
Nationwide within the United States
Code Information
SKUs: 900449; 916003; 916918; 901738; 916917; 999834; 902217; 916715
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1450-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026