Z-0441-05

Medtronic Midas Rex Legacy Telescoping Dissection Tool, Model TDQ-130D, manufactured by Medtronic Powered...

Name: Z-0441-05 Medtronic Midas Rex Legacy Telescoping Dissection Tool, Model TDQ-130D, manufactured by Medtronic Powered...
Creator: Power Surgical Solutions
Published: 2005-01-03
License: https://open.fda.gov/license/

Medtronic Powered Surgical Solutions / initiated 2005-01-03 / Terminated / root cause: packaging

FDA source

Power Surgical Solutions began a recall of Medtronic Midas Rex Legacy Telescoping Dissection Tool, Model TDQ-130D, manufactured by Medtronic Powered Surgical Solutions, Fort Worth, Texas 76137 on 2005-01-03. The reason FDA records is "Device is missing the sub-collet component within the dissecting tool package". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0441-05
Status: Terminated
Initiated: 2005-01-03
Posted: 2005-01-27
Terminated: 2005-11-03
Recalling firm: Medtronic Powered Surgical Solutions
Product: Medtronic Midas Rex Legacy Telescoping Dissection Tool, Model TDQ-130D, manufactured by Medtronic Powered Surgical Solutions, Fort Worth, Texas 76137
Product code: GET Motor, Surgical Instrument, Pneumatic Powered
Reason for recall: Device is missing the sub-collet component within the dissecting tool package.
Root cause tag: packaging
FDA root cause: Other
Action: The firm initiated the recall by letter on 01/03/2005. Firm representative will remove recalled product and replace with new product.
Quantity in commerce: 22 tools
Distribution: Product was distributed to three consignees in CA.
Product codes and lots: Lot Number 7087E

Product code GET

K953433Class IMidas Rex Telescoping SystemMidas Rex Pneumatic Tools, Inc. / cleared 1995-09-15

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)