Z-0514-06

Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016...

Name: Z-0514-06 Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016...
Creator: Hamilton Co
Published: 2005-12-13
License: https://open.fda.gov/license/

Hamilton Co / initiated 2005-12-13 / Terminated

FDA source

Hamilton Co began a recall of Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016, 135028, 135029, 936400, 936400BLU. Microlab AT+... on 2005-12-13. The reason FDA records is "Heat sinking on power boards may not operate as intended and the board may cease to operate". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0514-06
Status: Terminated
Initiated: 2005-12-13
Posted: 2006-02-14
Terminated: 2008-05-07
Recalling firm: Hamilton Co
Product: Microlab AT, part numbers 135001, 135001OOC, 135002, 135003, 135005, 135006, 135006R, 135007, 135008, 135016, 135028, 135029, 936400, 936400BLU. Microlab AT+ and Microlab AT+2, part numbers 142000, 142001, 142001R, 142002, 142003, 142005, 142006, 142006R, 142007, 142008, 142009, 142015, 142017, 142035, 142036
Product code: JTC Device, Microtiter Diluting/Dispensing
Reason for recall: Heat sinking on power boards may not operate as intended and the board may cease to operate.
FDA root cause: Other
Action: On 12/15/05, the firm initiated the recall and its notification was via letters explaining the reason for the recall and requesting the product be returned.
Quantity in commerce: 1071 units
Distribution: Product was released for distribution to 132 consignees in US, and 17 International consignees
Product codes and lots: All codes included.

Product code JTC

K871945Class IMicrolab atHamilton Co. / cleared 1987-05-29

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)