FDA Device recall Z-1256-2023
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location
- FDA Device
- Class II
- ongoing
- Published 2023-03-22
On 2023-03-22 the FDA classified a Class II recall of Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location by Stryker Medical Division, citing transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1256-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-02-01 |
| Published | 2023-03-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Reason
Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.
Identifiers
| code_info | GTIN: 07613327559118 Serial Numbers: 2208002066, 2208002071, 2209001508, 2208001664 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1256-2023%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.