Zinc Acetate — Class II drug recall D-1456-2016
Terminated recall by Spectrum Laboratory Products, Inc., reported 2016-08-17, distributed in GA, MA, MO, TN. Does not meet monograph: product exhibits lead levels in excess of the USP monograph limits.
| Recall number | D-1456-2016 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spectrum Laboratory Products, Inc., New Brunswick, NJ, United States |
| Recall initiated | 2016-08-01 |
| Classified | 2016-08-10 |
| Reported by FDA | 2016-08-17 |
| Terminated | 2017-04-07 |
| Distributed | GA, MA, MO, TN |
| Countries outside the US | CA |
| Quantity | 14,000 grams |
| Reason classes | chemical contamination |
| Lot numbers | 2EH0257 |
Product
Zinc Acetate, Crystal, USP, packaged in 500 gram bottles, Spectrum Chemical MFG, CORP., New Brunswick, NJ 08901
Reason for recall
Does not meet monograph: product exhibits lead levels in excess of the USP monograph limits.
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-1456-2016. 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.