CLASS II ONGOING Device recall · Reported 21 Jun 2023 · FDA Enforcement Report

Medicine Dropper, Product recalled by Apothecary Products

Apothecary Products is recalling Medicine Dropper, distributed nationwide in the US. The recall was initiated on 30 Mar 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number: 021623; UPC Number: 077602005085

Quantity recalled1,596 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1703-2023
FDA event ID: 92247
Recalling firm: Apothecary Products, Burnsville, MN
Classification: Class II
Status: Ongoing
Recall initiated: 30 Mar 2023
FDA classified: 9 Jun 2023
Reported: 21 Jun 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Particulate Matter
Device type: Masks, Gloves & PPE

Timeline

30 Mar 2023	Recall initiated by company
9 Jun 2023	Classified by FDA	+71 days
21 Jun 2023	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

Medicine Dropper, Product Code K508

Where it was 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.

Nationwide Alabama Arkansas Arizona California Colorado Florida Hawaii Illinois Indiana Missouri North Carolina New Jersey New York Oklahoma Oregon Pennsylvania Tennessee Texas Utah Washington

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot Number: 021623; UPC Number: 077602005085

Where was it sold?

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.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 92247

This product is part of a recall event; the main page for the event is Eye and Ear Dropper, Product recalled by Apothecary Products.

Reported	Class	Recall	Company	Reason	Where
21 Jun 2023	CLASS II	Eye and Ear Dropper, Product recalled by Apothecary Products	Apothecary Products	Particulate Matter	Nationwide

More recalls from Apothecary Products

All 2

Reported	Class	Recall	Company	Reason	Where
21 Jun 2023Device	CLASS II	Eye and Ear Dropper, Product recalled by Apothecary Products	Apothecary Products	Particulate Matter	Nationwide

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