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Terminated

Kuschall''s K3/K4 Series of Manual Wheelchair, Model Airlite.

FDA Recall Z-1486-06 · Posted 2006-09-06

Recalling FirmInvacare Corporation
Recall StatusTerminated
Product CodeIOR
Date Initiated2006-07-18
Date Terminated2012-03-01
Product Quantity208 wheelchairs

Reason for Recall

If the user has chosen to install optional anti-tippers on the chair, the anti-tipper as designed may not be able to bear the stress of repeated or quick loads placed on it, causing the bolt to bend or break.

Firm Action

The recalling firm notified all consignees by recall letter sent on or about 7/20/06 along with replacement anti-tippers for each device on hand.

Root Cause

Device Design

Distribution Pattern

Nationwide and Canada.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K982336KUSCHALL DESIGN K3/K4 SERIES OF MANUAL WHEELCHAIRSInvacare Corp. · 1998-08-21

Official Source

View FDA Recall →

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

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