Optikem International, Inc.: Drug Recall
Recall #D-0376-2024 · 02/29/2024
Class II: Risk
Recall Details
- Recall Number
- D-0376-2024
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Optikem International, Inc.
- Status
- Ongoing
- Date Initiated
- 02/29/2024
- Location
- Denver, CO, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7,248 bottles
Reason for Recall
Lack of Assurance of Sterility
Product Description
TRP Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-002-11.
Distribution Pattern
Product distributed Nationwide in the USA
Other Recalls by Optikem International, Inc.
- Class II: Risk 02/29/2024
- Class II: Risk 02/29/2024
- Class II: Risk 02/29/2024
- Class II: Risk 02/29/2024
- Class II: Risk 02/29/2024
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.