Recall Z-1734-2019— Maquet Cardiovascular Us Sales, Llc
Class II · Terminated
Class II FDA medical device recall by Maquet Cardiovascular Us Sales, Llc, initiated 2019-05-06, terminated 2022-07-06. FDA's recall record names no specific 510(k) clearance for this event. Product: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7) Part 710001F0 Product Usage: The Meera Mobile Operating Table is designed to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.. Reason: User may suffer an electric shock when coming in contact with the exposed electronic components.
- Recalling firm
- Maquet Cardiovascular Us Sales, Llc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-05-06
- Terminated
- 2022-07-06
- Firm location
- Wayne, NJ, United States
Product description
GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7) Part 710001F0 Product Usage: The Meera Mobile Operating Table is designed to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.
Reason for recall
User may suffer an electric shock when coming in contact with the exposed electronic components
Data sourced from openFDA. This site is unofficial and independent of the FDA.