Concentrated Motrin — Class II drug recall D-66272-001
Terminated recall by Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc., reported 2013-10-23, distributed nationwide. Presence of Foreign Substance: process-related particulates which may be associated with the raw materials wer
| Recall number | D-66272-001 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc., Fort Washington, PA, United States |
| Recall initiated | 2013-09-06 |
| Classified | 2013-10-17 |
| Reported by FDA | 2013-10-23 |
| Terminated | 2014-12-02 |
| Distributed | Nationwide (US) |
| Quantity | 197,532 bottles |
| Reason classes | specification failure |
| Lot numbers | DCB3T01, DDB4R01, DDB4S01 |
| Expiration dates | 2015-03-31 |
Product
Concentrated Motrin (ibuprofen) Infants' Drops Oral Suspension, Original Berry Flavor 1/2 fl oz bottles, 50 mg per 1.25ml, Distributed by McNeil Consumer Healthcare, Fort Washington, PA.
Reason for recall
Presence of Foreign Substance: process-related particulates which may be associated with the raw materials were observed
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-66272-001. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.