Drug recall
Blood Grouping Reagent, Anti-e (Human Monoclonal)(IgM)(For Further Manufacturing Use) EMD Millipore Catalog…
FDA recall event 63864 · Class III · Millipore (UK) Ltd.
Key facts
| Event ID | 63864 |
|---|---|
| Recall numbers | B-0725-13 |
| Recalling firm | Millipore (UK) Ltd. |
| Product type | Biologics |
| Products | Blood Grouping Reagent, Anti-e (Human Monoclonal)(IgM)(For Further Manufacturing Use) EMD Millipore Catalog Number: WD-1L-BK |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Single lot of Blood Grouping Reagent For Further Manufacturing Use, with a stability test point failure, was distributed. |
| Initiation date | Nov 20, 2012 |
| Report date | Jan 16, 2013 |
| Termination date | Jan 15, 2013 |
| City | Livingston |
| Country | United Kingdom |
| FEI number | 3002638287 |
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: