FDA Recalls MEERA CL Mobile Operating Tables for Unintended Movement Stops
Getinge Usa Sales Inc is recalling 112 MEERA CL mobile operating tables because error code 50037 may cause the table to stop moving unexpectedly when controlled via IR hand control, resulting in procedural delays.
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 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is a Class II device with no reported injuries, illnesses, or deaths. The stated consequence is procedural delay rather than direct patient harm. Without reported incidents and with only theoretical hazard, the severity is Moderate.
Plain-English summary
Getinge Usa Sales Inc is recalling the MEERA CL mobile operating table, a Class II medical device used for patient positioning during surgical procedures and examinations. The recall affects 112 units distributed nationwide in the United States and internationally to over 40 countries.
The recalled tables may experience error code 50037 on the IR-Hand Control, causing the table to stop moving unexpectedly. This malfunction may occur sporadically and can result in procedural delays during patient care.
Users of the MEERA CL operating table should contact Getinge Usa Sales Inc for information regarding this recall and any available corrective actions.
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: 710001B0
- Manufacturer
- Getinge Usa Sales Inc
- Affected units
- 112
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: 04046768136298 S/N: 680 through 707
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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