FDA Drug recall D-1372-2022
Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559
- FDA Drug
- Class II
- ongoing
- Published 2022-08-31
On 2022-08-31 the FDA classified a Class II recall of Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559 by Family Dollar Stores, citing CGMP Deviations: product held outside appropriate storage temperature conditions.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1372-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-23 |
| Published | 2022-08-31 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Family Dollar Stores |
| Distribution | US |
Product
Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559; TYLENOL CHILD GRAPE 4 FL OZ SKU 901600 TYLENOL CHILD ORAL SUSPENSION CHERRY 4 FO 913104 TYLENOL INFANTS DROPS DF CHERRY 1OZ SKU 999108 TYLENOL PM CAPLET 24 CT SKU 900603 TYLENOL EXTRA STRENGTH CAPLET 24 CT SKU 916986 TYLENOL 8HR MSL ACHE PAIN RD CAPLET 24 CT SKU 901155 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Reason
CGMP Deviations: product held outside appropriate storage temperature conditions.
Identifiers
| code_info | SKUs:900559; 901600; 913104; 999108; 900603; 916986; 901155 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1372-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.