Z-0844-05

Cool/Heat Versatility Main Controller Unit with 7-pin port only (for use with Thermal Resistive Type mattress)

Name: Z-0844-05 Cool/Heat Versatility Main Controller Unit with 7-pin port only (for use with Thermal Resistive Type mattress)
Creator: AMF Support Surfaces Inc
Published: 2005-01-27
License: https://open.fda.gov/license/

AMF Support Surfaces Inc / initiated 2005-01-27 / Terminated

FDA source

AMF Support Surfaces Inc began a recall of Cool/Heat Versatility Main Controller Unit with 7-pin port only (for use with Thermal Resistive Type mattress) on 2005-01-27. The reason FDA records is "Operator misconnected device power cords causing failure of the device". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0844-05
Status: Terminated
Initiated: 2005-01-27
Posted: 2005-05-17
Terminated: 2014-02-20
Recalling firm: AMF Support Surfaces Inc
Product: Cool/Heat Versatility Main Controller Unit with 7-pin port only (for use with Thermal Resistive Type mattress)
Product code: DWJ System, Thermal Regulating
Reason for recall: Operator misconnected device power cords causing failure of the device.
FDA root cause: Other
Action: Recall letters dated January 28, 2005, wee sent to consignees with instructions that a new control unit was being sent to their attention and directions for return of the previous control units.
Quantity in commerce: 6
Distribution: IN, MD, ND
Product codes and lots: Unit Serial Numbers 1020V0503E00174 1020V0304E00058 1020V0403E00145 1020V0203E00102 1020V0503E00088 1020V0403E00153

Product code DWJ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)