FDA Device recall Z-1703-2023
Medicine Dropper, Product Code K508
- FDA Device
- Class II
- ongoing
- Published 2023-06-21
On 2023-06-21 the FDA classified a Class II recall of Medicine Dropper, Product Code K508 by Apothecary Products, citing potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1703-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-30 |
| Published | 2023-06-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Apothecary Products |
| Distribution | US |
Product
Medicine Dropper, Product Code K508
Reason
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Identifiers
| upc | 077602005085 |
|---|---|
| code_info | Lot Number: 021623; UPC Number: 077602005085 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1703-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.