D-1393-2022 Class II Ongoing
FDA drug recall D-1393-2022 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
READY IN CASESLEEP AID SOFT GEL 32 CT SKU 901457 READY IN CASE SLEEP AID 64 CT SKU 999026 ZZZQUIL WARMING BERRY 12FL OZ SKU 999811 GOOD SENSESLEEP AID CAPLET 100 CT SKU 901496 GOOD SENSESLEEP AID CAPLET 24 CT SKU 913985 GOOD SENSE EZ NITE SLEEP BERRY 12FL OZSKU 999789 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: 901457; 999026; 999811; 901496; 913985; 999789
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1393-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026