FDA Device recall Z-1389-2018
Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and…
- FDA Device
- Class II
- terminated
- Published 2018-04-25
On 2018-04-25 the FDA classified a Class II recall of Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and… by Stryker Medical Division, citing the power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1389-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-12 |
| Published | 2018-04-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to assist with loading and unloading of a compatible wheeled stretcher (ambulance cot) to and from a transport vehicle and to secure the ambulance cot during transport. The device has a maximum safe working load of 870 lb (395 kg), which includes the weight of the ambulance cot, patient, and equipment attached to the cot (such as oxygen bottles, monitors, and pumps). The intended users of the device are trained professionals, including emergency medical service and medical care center personnel, as well as medical first responders, service technicians and installers.
Reason
The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.
Identifiers
| code_info | Serial numbers: 160139700 160139701 160139702 160139704…Serial numbers: 160139700 160139701 160139702 160139704 160139705 160139706 160139707 160139708 160139709 160139710 160139711 160139712 160139713 160139714 160139743 160139744 160139745 160139746 160139747 160139748 160139749 160139750 160139751 160139752 160139753 160139754 160139755 160139756 160139804 160139805 160139806 160139807 160139808 160139809 160139810 160139811 160139812 |
|---|
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-1389-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.