Device recall
Z-0547-2009: Bed Check Model #'s: BED65815-021 BED65815-025 BED65815-025IT BED65815-030…
FDA device recall · Class II · Sterilmed Inc
Key facts
| Recall number (Z-number) | Z-0547-2009 |
|---|---|
| Recall event | 49510 |
| Product | Bed Check Model #'s: BED65815-021 BED65815-025 BED65815-025IT BED65815-030 BED65815-031 BED73000 BED73010 BED74000 BED74010 NURBPP-30A NURBPP-30WC POS8283 RFT1000-1210 RFT1000-1250 RFT1000-1810 and RFT1000-1820 A bed-patient monitor is a battery-powered device placed under a mattress and used to… |
| Product code | KMI |
| Recalling firm | Sterilmed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2011 |
| FEI number | 3001237663 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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