Class II — Apothecary Products, LLC
| Recalling firm | APOTHECARY PRODUCTS, LLC |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. |
| Product | Eye and Ear Dropper, Product Code 67082 |
| Quantity | 2,346 units |
| Distribution | Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, HI, IL, IN, MO, NC, NJ, NY, OK, OR, PA, TN, TX, UT, WA and the country of Canada. |
| Initiated | 2023-03-30 |
| Classified | 2023-06-09 |
| Recall number | Z-1702-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Apothecary Products, LLC (Z-1702-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92247/
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