Atlas FDA

Pronto M51 Wheelchair, component- seat

FDA device recall Z-1400-06 · posted 2006-08-10 · Terminated

Recall details

Recalling firm
Invacare Corporation
Reason for recall
Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.
Action taken
The recalling firm sent a recall letter, dated 06/06 to consignees.
Root cause
Other
Status
Terminated
Product code
ITI
Quantity affected
853 units
Distribution
Nationwide.
Date initiated
2006-06-14
Date posted
2006-08-10
Date terminated
2007-08-22
Location
Elyria, OH

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Related 510(k) clearances

RecordFirmDate
INVACARE POWERED WHEELCHAIRS, MODELS M50, M51, M71 & M91 (K021680)Invacare Corp.2002-06-18