Drug recall
Refresh Tears (Carboxymethylcellulose Sodium Solution) 0.5%, Lubricant Eye Drops, Sterile packaged as 1) two…
FDA recall event 76861 · Class II · Cell Distributors
Key facts
| Event ID | 76861 |
|---|---|
| Recall numbers | D-0865-2017 |
| Recalling firm | Cell Distributors |
| Product type | Drugs |
| Products | Refresh Tears (Carboxymethylcellulose Sodium Solution) 0.5%, Lubricant Eye Drops, Sterile packaged as 1) two 15 mL bottles, USPC Code 784190442214, 2) 4x15 mL and one 5 mL bonus bottles, USPC Code… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling: Not elsewhere classified; product labeling lacks a NDC number, net weight information and does not contain the Drug Facts Panel. |
| Initiation date | Apr 3, 2017 |
| Report date | May 31, 2017 |
| Termination date | Jun 18, 2019 |
| City | Union |
| State | NJ |
| Country | United States |
| FEI number | 3011875637 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: