Drug recall
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND…
FDA recall event 77100 · Class II · PEROUSE MEDICAL
Key facts
| Event ID | 77100 |
|---|---|
| Recall numbers | Z-1891-2017 |
| Recalling firm | PEROUSE MEDICAL |
| Product type | Devices |
| Products | DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND 0185NA 0185ND |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Complaints regarding broken blister. |
| Initiation date | Apr 5, 2017 |
| Report date | May 10, 2017 |
| Termination date | Feb 1, 2021 |
| City | Ivry Le Temple |
| Country | France |
| FEI number | 3006942524 |
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: