Home / Recalls / Apothecary Products, LLC / Z-1702-2023

Z-1702-2023 Class II Ongoing

Recalled by Apothecary Products, LLC — Burnsville, MN

FDA device recall Z-1702-2023 was initiated by Apothecary Products, LLC on Mar 30, 2023 and is designated Class II. Reason for recall: Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb. The recall status is ongoing. Affected quantity: 2,346 units.

Recall details

Product Type: Devices
Report Date: Jun 21, 2023
Initiation Date: Mar 30, 2023
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2,346 units

Product description

Eye and Ear Dropper, Product Code 67082

Reason for recall

Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.

Distribution pattern

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.

Code information

Lot Number: 030923; UPC Number: 025715670829

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-1702-2023
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.