FDA Device recall Z-0479-2023
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US)
- FDA Device
- Class II
- ongoing
- Published 2022-12-21
On 2022-12-21 the FDA classified a Class II recall of Power-PRO 2, Model No. 6507, Item No. 650705550001 (US) by Stryker Medical Division, citing cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0479-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-11-11 |
| Published | 2022-12-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Reason
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Identifiers
| code_info | UDI-DI (GTIN) 07613327504460 Serial Numbers 2204000343 2204000345 2204000348…UDI-DI (GTIN) 07613327504460 Serial Numbers 2204000343 2204000345 2204000348 2204000351 2204000369 2204000370 2204000382 2204000430 2204000673 2204000682 2205000094 2205000095 2205000096 2205000097 2205000098 2205000099 2205000100 2205000101 2205000102 2205000104 2205000105 2205000109 2205000110 2205000111 2205000113 2205000115 2205000117 2205000119 2205000123 2205000124 2205000125 2205000128 2205000129 2205000130 2205000132 2205000135 22050001 |
|---|
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-0479-2023%22
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