Z-1698-2009

Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Dover...

Name: Z-1698-2009 Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Dover...
Creator: Zimmer Inc.
Published: 2009-06-08
License: https://open.fda.gov/license/

Zimmer GmbH / initiated 2009-06-08 / Terminated / root cause: packaging

FDA source

Zimmer Inc. began a recall of Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Dover, Ohio; Catatog Number: 00515018300. Used in conjunction... on 2009-06-08. The reason FDA records is "The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility". 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-1698-2009
Status: Terminated
Initiated: 2009-06-08
Posted: 2009-07-23
Terminated: 2009-12-15
Recalling firm: Zimmer GmbH
Product: Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Dover, Ohio; Catatog Number: 00515018300. Used in conjunction with the Pulsavac Plus Wound Debridement System for pulsatile lavage/debridement.
Product code: FQH Lavage, Jet
Reason for recall: The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.
Root cause tag: packaging
FDA root cause: Packaging process control
Action: Zimmer Orthopedic Surgical Products issued an "Urgent: Medical Device Recall" notice dated June 8, 2009 informing users of the affected devices and actions to be taken including the return of product and acknowledgement of receipt of notice by returning the Recall Certification Form by fax to 1-330-364-0974.
Quantity in commerce: 15
Distribution: Worldwide Distribution -- United States, Canada and Japan.
Product codes and lots: Lot Number: 61229259.

Product code FQH

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 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)