Family Dollar Stores product recalled over manufacturing violations
- Recall date
- June 23, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Family Dollar Stores, Llc. recalls READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 REA…
- Recall number
- D-1392-2022
- FDA classification
- Class II
- Brand / firm
- Family Dollar Stores, Llc.
- Sold / distributed
- Nationwide within the United States
Why it was recalled
CGMP Deviations: product held outside appropriate storage temperature conditions.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
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