Recall Z-0424-2024— Stryker Medical Division of Stryker Corporation
Class II · Ongoing
Class II FDA medical device recall by Stryker Medical Division of Stryker Corporation, initiated 2023-08-30. FDA's recall record names no specific 510(k) clearance for this event. Product: ProCuity bed series, model number 3009, item number: 300900000000,. Reason: Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock..
- Recalling firm
- Stryker Medical Division of Stryker Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-08-30
- Firm location
- Portage, MI, United States
Product description
ProCuity bed series, model number 3009, item number: 300900000000,
Reason for recall
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Data sourced from openFDA. This site is unofficial and independent of the FDA.