The Recall Desk
HighFDA (Devices)·Z-1703-2023·Announced 2023-06-21

Medicine Dropper Recalled for Potential Glass Particulate Contamination

Apothecary Products, LLC is recalling 1,596 units of Medicine Dropper (Lot 021623) due to potential glass particles on the dropper bulb exterior. Glass particles could contaminate medication or cause injury.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: This is an FDA Class II medical device recall for potential glass contamination. Glass particles on the dropper exterior present a risk of medication contamination or laceration, meeting the High (3) threshold for risk-of-harm products.

Plain-English summary

Apothecary Products, LLC is recalling 1,596 units of Medicine Dropper, Product Code K508 (Lot Number 021623, UPC 077602005085). The dropper bulbs may have glass particles on their exterior surfaces.

Glass particles on the dropper's outside surface present a potential risk of contaminating medication being dispensed or causing injury when handling the dropper.

The affected product was distributed nationwide in 20 US states (AL, AR, AZ, CA, CO, FL, HI, IL, IN, MO, NC, NJ, NY, OK, OR, PA, TN, TX, UT, WA) and Canada.

The recalled product

Product
Medicine Dropper, Product Code K508
Affected units
1,596

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot Number: 021623
  • UPC Number: 077602005085

Distribution

Distributed nationwide across the United States.

The notice also names 20 states specifically:

Part of a larger recall action

This product is one of 2 recalled by Apothecary Products, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 2 products in this recall →

Same manufacturer · Apothecary Products, LLC

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