Atlas FDA

Invacare 2G Tarsys Seating System, Model 2GR.

FDA device recall Z-0343-04 · posted 2004-01-14 · Terminated

Recall details

Recalling firm
Invacare Corporation
Reason for recall
The weld joints on the seat back may fail and cause possible injury to the patient.
Action taken
The firm notified their consignees by letter and telephone on 12/15/2003.
Root cause
Other
Status
Terminated
Product code
ITI
Quantity affected
5,990 units
Distribution
The units were shipped to domestic dealerships located nationwide, and to foreign accounts in Canada, China, Oman, and West Indies.
Date initiated
2003-12-15
Date posted
2004-01-14
Date terminated
2008-09-13
Location
Elyria, OH

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