Drug recall
V6400 Invasive Pressure Monitor uses WW3005 power cord. (Electri-Cord Manufacturing Co.,312 E. Main St…
FDA recall event 54361 · Class II · Smiths Medical PM, Inc.
Key facts
| Event ID | 54361 |
|---|---|
| Recall numbers | V-033-2010, V-034-2010, V-035-2010 |
| Recalling firm | Smiths Medical PM, Inc. |
| Product type | Veterinary |
| Products | V6400 Invasive Pressure Monitor uses WW3005 power cord. (Electri-Cord Manufacturing Co.,312 E. Main St., Westfield, PA 16950)., V8400 Capnocheck Capnometer utilizes the power cord 8404 for its battery charger (Electri-Cord Manufacturing Co.,312 E. Main St., Westfield, PA 16950)., V9200 Advisor Vital Signs Monitor utilizes the power cord WW3005 (Electri-Cord Manufacturing Co.,312 E. Main St., Westfield, PA 16950). |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Smiths Medical is conducting a voluntary recall of a limited number of medical device AC power cords, manufactured by Electri-Cord manufacturing Co., for use with BCI 3180 Pulse Oximeter(Human), 9200… |
| Initiation date | Jan 15, 2010 |
| Termination date | Mar 14, 2012 |
| City | Waukesha |
| State | WI |
| Country | United States |
| FEI number | 2182466 |
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