Drug recall
Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part
FDA recall event 87657 · Class I · Infusion Pump Repair
Key facts
| Event ID | 87657 |
|---|---|
| Recall numbers | Z-1544-2021 |
| Recalling firm | Infusion Pump Repair |
| Product type | Devices |
| Products | Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of… |
| Initiation date | Mar 26, 2021 |
| Report date | May 19, 2021 |
| City | Irvine |
| State | CA |
| Country | United States |
| FEI number | 3011655432 |
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: