Z-0102-06

Accumetrics part number 29001 VerifyNow Instrument, printe power supply

Name: Z-0102-06 Accumetrics part number 29001 VerifyNow Instrument, printe power supply
Creator: Accumetrics Inc
Published: 2005-09-13
License: https://open.fda.gov/license/

Accumetrics, Inc. / initiated 2005-09-13 / Terminated

FDA source

Accumetrics Inc began a recall of Accumetrics part number 29001 VerifyNow Instrument, printe power supply on 2005-09-13. The reason FDA records is "In 2001, separate reports of mild shock, sparking and smoke from Accumetrics PN 29001 power supply". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0102-06
Status: Terminated
Initiated: 2005-09-13
Posted: 2005-10-28
Terminated: 2007-03-03
Recalling firm: Accumetrics, Inc.
Product: Accumetrics part number 29001 VerifyNow Instrument, printe power supply
Product code: JOZ System, Automated Platelet Aggregation
Reason for recall: In 2001, separate reports of mild shock, sparking and smoke from Accumetrics PN 29001 power supply.
FDA root cause: Other
Action: Letters and replacement power supplies were sent to consignees by Fedex, 2-day with proof of delivery. End-user customers were instructed to return the affected power supply to Accumetrics, using the provided pre-paid shipping carton. Consignees who do not return the power supply within two weeks of the notification will be contacted by phone to assess compliance with the recall and to determine the status of the product at the site.
Quantity in commerce: 11
Distribution: CA, FL, IL, LA, NH, NV, NY, OK, WA
Product codes and lots: lot number G-13850

Product code JOZ

K992531Class IIUltegra System Analyzer, Ultegra System Rpfa-Trap Test Cartidges, Ultegra System Rpfa-Trap Level One Qc, Ultegra SystemAccumetrics, Inc. / cleared 1999-12-20

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)