Maquet Cardiovascular Us Sales, Llc 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Maquet Cardiovascular Us Sales, Llc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
(1) Part 720001B2 S/N 1 to S/N 416 (2) Part 720001B0 S/N 1 to S/N 1416 (3) Part 720001F2 S/N 1 to S/N 91 (4) Part 720001F0 S/N 1 to S/N 220 (5) Part 710001B2 S/N 1 to S/N 8 (6) Part 710001B0 S//N 1 to S/N 11 (7) Part 710001F0 S/N 1 Expanded lots: 720001B2 SN 417 to SN 503 720001B0 SN 1417 to SN 1689 720001F2 SN 92 to SN 119 720001F0 SN 221 to SN 226 and SN 701 to 711 710001B2 SN 9 to SN 14 710001B0 SN 12 to SN 88
Maquet Cardiovascular Us Sales, Llc is recalling GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 ( due to User may suffer an electric shock when coming in contact with the exposed electronic components. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
User may suffer an electric shock when coming in contact with the exposed electronic components
Recommended Action
Per FDA guidance
Maquet /Getinge issued URGENT MEDICAL DEVICE CORRECTION Notice on 5/6/19, identified issued, health risk and action to take: Per the IFU, section 8.1, a visual and functional check is required to be performed by a trained person before operation; If the plastic socket of the cold-device plug is pulled out do not try to put it back into the housing and if there are any exposed electronic components: do not touch them. Call your in-house technical service and arrange the repair of the table. Per IFU section 8.5 a defective product may not be used and may not be repaired by yourself. Complete/sign and return the MEDICAL DEVICE RECALL CORRECTION RESPONSE FORM. Questions contact Technical Support Department at 1-888-627-8383 (press option 3 then option 1), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. EST. Expanded Recall: Maquet/Getinge issued letters on 9/24/20 to consignees via FedEx 2 day Delivery with Signature Proof of Delivery (SPOD).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026