Device recall
Z-0072-2012: ***REF #250***TAPSCOPE 550F. Each pouch contains one (1) 18 French esophageal…
FDA device recall · Class II · Cardiocommand Inc.
Key facts
| Recall number (Z-number) | Z-0072-2012 |
|---|---|
| Recall event | 58302 |
| Product | ***REF #250***TAPSCOPE 550F. Each pouch contains one (1) 18 French esophageal stethoscope with bipolar pacing and recording electrodes with a YSI 400 series female connector thermistor. LOT xxxxxxx 400095-0250-C 100902. www.cardiocommand.com. ***REF #250-0010***TAPSCOPE 550F CONTAINS: Ten (10) 18… |
| Product code | LPA |
| Recalling firm | Cardiocommand Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2012 |
| PMA numbers | P860008 |
| FEI number | 1927197 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database