Sanarus Medical Inc Sanarus Visica Treatment System (disposable), Model/Product Code: VP-0500 (single) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sanarus Visica Treatment System (disposable), Model/Product Code: VP-0500 (single)
Brand
Sanarus Medical Inc
Lot Codes / Batch Numbers
Lot # C030404
Products Sold
Lot # C030404
Sanarus Medical Inc is recalling Sanarus Visica Treatment System (disposable), Model/Product Code: VP-0500 (single) due to Corrosion in stainless steel device shaft that allows Argon gas to escape from device during a cryoablation procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Corrosion in stainless steel device shaft that allows Argon gas to escape from device during a cryoablation procedure.
Recommended Action
Per FDA guidance
A recall notification letter was sent via Federal Express to all affected customers on 06/16/2003.
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