Drug recall
Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use…
FDA recall event 76661 · Class III · Pharmedium Services, LLC
Key facts
| Event ID | 76661 |
|---|---|
| Recall numbers | D-0603-2017 |
| Recalling firm | Pharmedium Services, LLC |
| Product type | Drugs |
| Products | Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered Lidocaine 1% instead of correctly as Buffered Lidocaine 0.9% |
| Initiation date | Jan 27, 2017 |
| Report date | Mar 22, 2017 |
| Termination date | Mar 16, 2017 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3005051736 |
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: