Equate Night-time Sleep Aide — Class II drug recall D-1630-2019
Terminated recall by LNK International, Inc., reported 2019-08-07, distributed nationwide. Microbial contamination of non-sterile product
| Recall number | D-1630-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LNK International, Inc., Hauppauge, NY, United States |
| Recall initiated | 2019-07-10 |
| Classified | 2019-08-06 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2023-06-09 |
| Distributed | Nationwide (US) |
| Reason classes | microbial contamination, sterility |
| NDC | 49035-0330, 49035-0330-02, 49035-0330-45, 49035-0330-96 |
| Lot numbers | P300456, P300475, P300482, P300489 |
| Expiration dates | 2020-09-30 |
Product
Equate Night-time Sleep Aide (Diphenhydramine HCl), 50 mg, Alcohol Free, Berry Flavor, 12 Fl. Oz. (354 mL), OTC, Distributed by: Walmart Stores, Inc., Bentonville, AR 72716, NDC 49035-330-02, UPC 6 8113117595 1
Reason for recall
Microbial contamination of non-sterile product
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-1630-2019. 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.