Medical device recalls Moderate risk

Apothecary Products, LLC recalls Eye and Ear Dropper, Product Code 67082

Recall date
March 30, 2023
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1702-2023
FDA classification
Class II
Brand / firm
Apothecary Products, LLC
Sold / distributed
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.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Eye and Ear Dropper, Product Code 67082

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