Z-2114-2010

Microwave Ovens, Model Number DG-2

Name: Z-2114-2010 Microwave Ovens, Model Number DG-2
Creator: Duke Manufacturing Co.
Published: 2010-05-12
License: https://open.fda.gov/license/

Duke Manufacturing Co. / initiated 2010-05-12 / Terminated

FDA source

Duke Manufacturing Co. began a recall of Microwave Ovens, Model Number DG-2 on 2010-05-12. The reason FDA records is "The oven did not meet Federal Performance Standard for certain requirements". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-2114-2010
Status: Terminated
Initiated: 2010-05-12
Posted: 2010-09-12
Terminated: 2012-04-17
Recalling firm: Duke Manufacturing Co.
Product: Microwave Ovens, Model Number DG-2
Product code: RCS Microwave Oven, Commercial
Reason for recall: The oven did not meet Federal Performance Standard for certain requirements.
FDA root cause: Radiation Control for Health and Safety Act
Action: Letters were sent to Duke Manufacturing Speed Oven Owners. The letters identified the affected product and stated the reason for recall. The letter also states that the firm instituted a repair program on all DG-2 Speed Ovens. The firm will repair of replace all affected products at no charge to the customer. Customer Service personnel will contact customers directly and coordinate the schedule of the required repairs.
Quantity in commerce: 62 units
Distribution: Nationwide Distribution
Product codes and lots: Accession number: 0930317-000

Product code RCS

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)