Medicine Dropper — Class II medical device recall Z-1703-2023
Ongoing recall by Apothecary Products, LLC, reported 2023-06-21, distributed nationwide. Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
| Recall number | Z-1703-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apothecary Products, LLC, Burnsville, MN, United States |
| Recall initiated | 2023-03-30 |
| Classified | 2023-06-09 |
| Reported by FDA | 2023-06-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,596 units |
| Reason classes | foreign material, specification failure |
| UPC / GTIN / UDI-DI | 00077602005085 |
| Lot numbers | 021623 |
Product
Medicine Dropper, Product Code K508
Reason for recall
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
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/Z-1703-2023. 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.