MEERA CL Mobile Operating Table Control Malfunction Recall
The MEERA CL mobile operating table may experience error code 50037 that stops table movement during use, causing surgical procedure delays. Getinge recalled 342 units distributed worldwide.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II medical device classified as a risk-of-harm product (operating table used in surgical settings). No injuries, hospitalizations, or deaths are reported. The scoring reflects the functional malfunction risk in a critical care environment without documented patient harm.
Plain-English summary
Getinge Usa Sales Inc is recalling 342 units of the MEERA CL mobile operating table. The device is designed for patient positioning immediately before, during, and after surgical procedures, as well as for examination and treatment.
Error code 50037 may occur sporadically when the table is controlled via the IR-Hand Control. When this error occurs, the operating table stops its movement, which may result in procedural delays.
The recalled units have serial numbers ranging from 11399 through 11746 and are identified by UDI-DI: 04046768124332. The devices have been distributed worldwide, including to the United States and numerous international locations.
The recalled product
- Product
- MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, Item Number: 720001B0
- Manufacturer
- Getinge Usa Sales Inc
- Affected units
- 342
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UDI-DI: 04046768124332 S/N: 11399 through 11746
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 8 recalled by Getinge Usa Sales Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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