FDA Device recall Z-0517-2018
PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3
- FDA Device
- Class II
- terminated
- Published 2018-02-14
On 2018-02-14 the FDA classified a Class II recall of PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3 by Panoramic Rental, citing the lift motor used to raise and lower the overhead chassis will wear if not properly maintained according to the maintenance schedule.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0517-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-14 |
| Published | 2018-02-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Panoramic Rental |
| Distribution | US |
Product
PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3
Reason
The lift motor used to raise and lower the overhead chassis will wear if not properly maintained according to the maintenance schedule.
Identifiers
| code_info | Serial Numbers: 6001 to 19340 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0517-2018%22
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