Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Invacare 2G Tarsys Seating System, Model 2GR.

FDA Recall Z-0343-04 · Posted 2004-01-14

Recalling FirmInvacare Corporation
Recall StatusTerminated
Product CodeITI
Date Initiated2003-12-15
Date Terminated2008-09-13
Product Quantity5,990 units

Reason for Recall

The weld joints on the seat back may fail and cause possible injury to the patient.

Firm Action

The firm notified their consignees by letter and telephone on 12/15/2003.

Root Cause

Other

Distribution Pattern

The units were shipped to domestic dealerships located nationwide, and to foreign accounts in Canada, China, Oman, and West Indies.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑