Recall Z-1702-2023— Apothecary Products, LLC
Class II · Ongoing
Class II FDA medical device recall by Apothecary Products, LLC, initiated 2023-03-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Eye and Ear Dropper, Product Code 67082. Reason: Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb..
- Recalling firm
- Apothecary Products, LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-03-30
- Firm location
- Burnsville, MN, United States
Product description
Eye and Ear Dropper, Product Code 67082
Reason for recall
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
Data sourced from openFDA. This site is unofficial and independent of the FDA.