MAQUET Inc. Maquet Servo Ventilator SV900C/D/E (SV900) Siemens-Elema AB, Solna, Sweden Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Maquet Servo Ventilator SV900C/D/E (SV900) Siemens-Elema AB, Solna, Sweden
Brand
MAQUET Inc.
Lot Codes / Batch Numbers
Serial Numbers 010001-188499 Ventilators within the specified serial number range, 2. Upgrade SV300 6682-745 SV900 66 82 747.
Products Sold
Serial Numbers 010001-188499 Ventilators within the specified serial number range, that are marked with one of the following labels on the inside of the lid of the pneumatic unit are exempted since they have already been fitted with a new type of the pressure transducer. 1. Upgrade EMO 12/02/1; 2. Upgrade SV300 6682-745 SV900 66 82 747.
MAQUET Inc. is recalling Maquet Servo Ventilator SV900C/D/E (SV900) Siemens-Elema AB, Solna, Sweden due to Some Servo Ventilators 300/300A and Servo Ventilator 900C/D/E should not be used with a system that may generate negative pressure below -100 cm H2O (. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some Servo Ventilators 300/300A and Servo Ventilator 900C/D/E should not be used with a system that may generate negative pressure below -100 cm H2O (Closed system suctioning) due to the risk of damaging the ventilator's pressure transducers.
Recommended Action
Per FDA guidance
Maquet sent Device Correction letters commencing 11/17/09 and ending 11/23/09 by Federal Express.
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