Device recall
Z-0285-2016: Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051…
FDA device recall · Class II · ErgoSafe Products, LLC (DBA) Prism Medical
Key facts
| Recall number (Z-number) | Z-0285-2016 |
|---|---|
| Recall event | 71680 |
| Product | Prism Medical P-300 Portable Consumer Lift; PN 303050, 303050R, and 303051; weight specification 300 lbs. /136 kg. |
| Product code | FSA |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2017 |
| FEI number | 3007802293 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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