Zimmer Inc. 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Zimmer Inc.
Lot Codes / Batch Numbers
Lot Number: 61229259.
Products Sold
Lot Number: 61229259.
Zimmer Inc. is recalling Zimmer Pulsavac Wound Debridement System high capacity intramedullary brush tip, sterile, Zimmer, Do due to The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The seal on the sterile barrier pouch may be inadequate, resulting in lack of assurance of sterility.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026