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  5. FDA Recall: Blur Relief

FDA Recall Blur Relief

View Recall Number, Date, Reasons, Quantity

FDA Recall Enforcement Reports

The last Recall Enforcement Report for Blur Relief with NDC 17312-002 was initiated on 02-29-2024 as a Class II recall due to lack of assurance of sterility The latest recall number for this product is D-0376-2024 and the recall is currently ongoing .

Recall Number Initiation Date Report Date Recall Classification Product Quantity Product Description Status
D-0376-202402-29-202403-20-2024Class II7,248 bottlesTRP 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.Ongoing
D-1154-202309-01-202309-27-2023Class II5,509TRP Natural Eyes, Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-002-11.Ongoing
D-0469-202007-02-201911-27-2019Class II24144 unitsTRP Blur Relief, 15 mL, NDC 17312-002-11Ongoing

What is the Enforcement Report?

All drug recalls are monitored by the Food and Drug Administration (FDA) and are included in the Enforcement Report once they are properly classified. The FDA will determine if a firm's removal or correction actions of a marked product meet the requirements to be considered a "recall". The FDA will also determine the public hazard assessment and a recall classification will be published in the Enforcement Report.