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Terminated

Pronto M51 Wheelchair, component- seat

FDA Recall Z-1400-06 · Posted 2006-08-10

Recalling FirmInvacare Corporation
Recall StatusTerminated
Product CodeITI
Date Initiated2006-06-14
Date Terminated2007-08-22
Product Quantity853 units

Reason for Recall

Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.

Firm Action

The recalling firm sent a recall letter, dated 06/06 to consignees.

Root Cause

Other

Distribution Pattern

Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K021680INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91Invacare Corp. · 2002-06-18

Official Source

View FDA Recall →

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

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