Drug recall
Allergenic Extracts
FDA recall event 75433 · Class III · Greer Laboratories Inc
Key facts
| Event ID | 75433 |
|---|---|
| Recall numbers | B-0077-2017, B-0078-2017 |
| Recalling firm | Greer Laboratories Inc |
| Product type | Biologics |
| Products | Allergenic Extracts, Juniper, Western |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Allergenic Extracts, labeled with an incorrect PNU measurement, were distributed. |
| Initiation date | Sep 16, 2016 |
| Report date | Oct 19, 2016 |
| Termination date | Oct 13, 2016 |
| City | Lenoir |
| State | NC |
| Country | United States |
| FEI number | 1011574 |
At a glance
- 1–9 Products in this recall
- 10–99 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: