Eye and Ear Dropper, Product Code 67082
FDA device recall Z-1702-2023 · posted 2023-06-09 · Open, Classified
Recall details
- Recalling firm
- Apothecary Products, LLC
- Reason for recall
- Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.
- Action taken
- Apothecary Products notified customers on 03/31/2023 via email. Customers were instructed to immediately check inventory and discard the affected units, notify customers if further distributed, and complete and return the Customer Response Acknowledgement Notification.
- Root cause
- Process control
- Status
- Open, Classified
- Product code
- KCM
- Quantity affected
- 2,346 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.
- Date initiated
- 2023-03-30
- Date posted
- 2023-06-09
- Location
- Burnsville, MN
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