RecallRadar

FDA Drug recall D-1392-2022

READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN R…

On 2022-08-31 the FDA classified a Class II recall of READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN R… by Family Dollar Stores, citing CGMP Deviations: product held outside appropriate storage temperature conditions.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1392-2022
ClassificationClass II
Statusongoing
Initiated2022-06-23
Published2022-08-31
Last updated2026-09-13 11:52 UTC
CompanyFamily Dollar Stores
DistributionUS

Product

READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN RELIEVER CAPLET 50 CT SKU 913982 GOOD SENSE PAIN RELIEVER APAP ES 500 CT SKU 999029 GOOD SENSE PAIN RELIEVER CAPLET 100 CT SKU 913890 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_infoSKUs: 902381; 902332; 913982; 999029; 913890

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-1392-2022%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.