Homeocare Laboratories, Inc.: Drug Recall
Recall #D-0884-2023 · 06/05/2023
Class II: Risk
Recall Details
- Recall Number
- D-0884-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Homeocare Laboratories, Inc.
- Status
- Terminated
- Date Initiated
- 06/05/2023
- Location
- Yonkers, NY, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 12,850 tottles
Reason for Recall
cGMP deviations
Product Description
DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15
Distribution Pattern
Product was distributed USA nationwide.
Other Recalls by Homeocare Laboratories, Inc.
- Class II: Risk 06/05/2024
- Class I: Dangerous 06/05/2024
- Class II: Risk 06/05/2023
- Class II: Risk 06/05/2023
- Class II: Risk 06/05/2023
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.