Atlas FDA

Mattress Model 5185 and 5185XL. Manufactured by: Invacare Corp., 2101 East Lake Mary Blvd., Sanford, FL 32773. Mattress

FDA device recall Z-2403-2010 · posted 2010-09-12 · Terminated

Recall details

Recalling firm
Invacare Corporation
Reason for recall
In September 2007 Invacare Corporation recalled the innerspring mattresses associated with Invacare's IVC Bed Series Full Electric Beds, Semi-Electric Beds and Manual Beds and the ValueCare Bed Series Semi Electric Bed. These mattresses were manufactured between June 28, 2007 and July 12, 2007. These mattresses when used in combination with the IVC and ValueCare Series of manual, semi-electric a
Action taken
Consignees of the product were notified by letter dated 09/05/2007. Consignees were instructed to destroy the affected mattresses and to return the completed confirmation of the destruction form to Invacare.
Root cause
Device Design
Status
Terminated
Product code
FMW
Quantity affected
4896
Distribution
Nationwide Distribution
Date initiated
2007-08-29
Date posted
2010-09-12
Date terminated
2010-09-13
Location
Sanford, FL

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