Z-0602-06

Thermoplastic templates, single tooth Catalog Number: 040.526

Name: Z-0602-06 Thermoplastic templates, single tooth Catalog Number: 040.526
Creator: Straumann Manufacturing Inc.
Published: 2006-01-30
License: https://open.fda.gov/license/

Straumann USA, LLC / initiated 2006-01-30 / Terminated

FDA source

Straumann Manufacturing Inc. began a recall of Thermoplastic templates, single tooth Catalog Number: 040.526 on 2006-01-30. The reason FDA records is "Pilot drills may not fully extend through drill guide in template products". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0602-06
Status: Terminated
Initiated: 2006-01-30
Posted: 2006-03-09
Terminated: 2006-05-04
Recalling firm: Straumann USA, LLC
Product: Thermoplastic templates, single tooth Catalog Number: 040.526
Product code: DZJ Driver, Wire, And Bone Drill, Manual
Reason for recall: Pilot drills may not fully extend through drill guide in template products
FDA root cause: Other
Action: Straumann USA notified consignees by letter dated 1/30/06 requesting return of the devices.
Quantity in commerce: 116
Distribution: Nationwide
Product codes and lots: Lot Number: A2283

Product code DZJ

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)