Z-0672-06

Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; Part...

Name: Z-0672-06 Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; Part...
Creator: Zimmer Inc.
Published: 2006-02-02
License: https://open.fda.gov/license/

Zimmer GmbH / initiated 2006-02-02 / Terminated

FDA source

Zimmer Inc. began a recall of Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; Part number 00-7712-035-02 on 2006-02-02. The reason FDA records is "A c-clip located near the rasp connection end of the instrument may detach during use and fall into the patient". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0672-06
Status: Terminated
Initiated: 2006-02-02
Posted: 2006-03-21
Terminated: 2007-12-05
Recalling firm: Zimmer GmbH
Product: Zimmer Minimally Invasive Solutions Technology Offset Rasp Handle, Right, 45 degrees, non-sterile; Part number 00-7712-035-02.
Product code: LXH Orthopedic Manual Surgical Instrument
Reason for recall: A c-clip located near the rasp connection end of the instrument may detach during use and fall into the patient.
FDA root cause: Other
Action: Firm sales personnel were notified by letter dated 2/8/06 to visit each of their affected accounts and to remove the c-clip from the rasps or to remove the instrument from the hospital and return it to the firm. Similar instructions issued by letter dated 2/27/06 when the recall was extended to the two additional products.
Quantity in commerce: 495 Right and Left
Distribution: Nationwide, Australia, Canada, Germany, Korea, Singapore and Taiwan.
Product codes and lots: Lots 60244777, 60254446, 60259343, 60280558, 60295662, 60298480, 60307612, 60333170 and 60336853.

Product code LXH

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)