Z-1141-04

Microvent Implant Line

Name: Z-1141-04 Microvent Implant Line
Creator: Zimmer Dental Inc
Published: 2004-01-13
License: https://open.fda.gov/license/

ZimVie US Corp LLC / initiated 2004-01-13 / Terminated / root cause: sterility

FDA source

Zimmer Dental Inc began a recall of Microvent Implant Line on 2004-01-13. The reason FDA records is "Sterility barrier compromised". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as sterility.

Recall record

Recall number: Z-1141-04
Status: Terminated
Initiated: 2004-01-13
Posted: 2004-07-23
Terminated: 2004-09-01
Recalling firm: ZimVie US Corp LLC
Product: Microvent Implant Line
Product code: DZE Implant, Endosseous, Root-Form
Reason for recall: Sterility barrier compromised.
Root cause tag: sterility
FDA root cause: Other
Quantity in commerce: See Codes
Product codes and lots: MicroVent Implant Line Part # Description Lot Number Quantity MV3H10 Impl, M-V II, HA, 3.7mm, 10mm 0200515 100 MV3H10 Impl, M-V II, HA, 3.7mm, 10mm 0202923 100 MV3H13 Impl, M-V II, HA, 3.7mm, 13mm 014962 270 MV3H13 Impl, M-V II, HA, 3.7mm, 13mm 0200428 200 MV3H8 Impl, M-V II, HA, 3.7mm, 8mm 0202162 30 MV4H10 Impl, M-V II, HA, 4.7mm, 10mm 0200516 100 MV4H13 Impl, M-V II, HA, 4.7mm, 13mm 016646 100 MV4H13 Impl, M-V II, HA, 4.7mm, 13mm 0200427 100 MV4H8 Impl, M-V II, HA, 4.7mm, 8mm 0201180 35

Product code DZE

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)