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Open, Classified

Eye and Ear Dropper, Product Code 67082

FDA Recall Z-1702-2023 · Posted 2023-06-09

Recalling FirmApothecary Products, LLC
Recall StatusOpen, Classified
Product CodeKCM
Date Initiated2023-03-30
Product Quantity2,346 units

Reason for Recall

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

Firm Action

Apothecary Products notified customers on 03/31/2023 via email. Customers were instructed to immediately check inventory and discard the affected units, notify customers if further distributed, and complete and return the Customer Response Acknowledgement Notification.

Root Cause

Process control

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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