Drug recall
Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC…
FDA recall event 84326 · Class II · SCA Pharmaceuticals, LLC
Key facts
| Event ID | 84326 |
|---|---|
| Recall numbers | D-0620-2020 |
| Recalling firm | SCA Pharmaceuticals, LLC |
| Product type | Drugs |
| Products | Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Presence of Foreign Substance: Foreign material found inside the vial (manufacturer). |
| Initiation date | Nov 26, 2019 |
| Report date | Dec 18, 2019 |
| Termination date | Feb 7, 2020 |
| City | Windsor |
| State | CT |
| Country | United States |
| FEI number | 3013736415 |
At a glance
- 1–9 Products in this recall
- 1–9 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: