FDAClass IIJune 21, 2023

Medicine Dropper recall: Particulate Matter

Medicine Dropper, Product Code K508

Why was Medicine Dropper recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Number: 021623; UPC Number: 077602005085

Product
Medicine Dropper, Product Code K508
Recalling firm
Apothecary Products, LLC
Quantity
1,596 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.
Recall date
June 21, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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