Sonesta Medical Ab: Medical Device Recall in 2017 - (Recall #: Z-1894-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V

Product Classification:

Class II

Date Initiated: March 8, 2017

Date Posted: May 10, 2017

Recall Number: Z-1894-2017

Event ID: 77075

Reason for Recall:

The user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient weight.

Status: Terminated

Product Quantity: 28 devices

Code Information:

12-00001-110V 12-00011-110V 23-00002-220V (Demo Product) 12-00002-110V 12-00012-110V 23-00001-220V 12-00003-110V 12-00013-110V 23-00003-220V 12-00004- 110V 12-00014-110V 23-00004-220V 12-00005-110V 12-00015-110V 23-00005-220V 12-00006-110V 12-20001-110V 23-00006-220V 12-00007-110V 12-20002-110V 23-00009-220V 12-00008-110V 12-20003-110V 23-00020-220V 12-00009-110V 12-20004 -110V 23-20001-220V 12-00010-110V 23-20002-220V

Distribution Pattern:

Worldwide Distribution - US Distribution to the state of : MA., and to the countries of : Canada, Netherlands, Dubai, Taiwan, Lebanon, Italy

Voluntary or Mandated:

Voluntary: Firm initiated