Medical Devices
Phoenix Biomedical Cruciform Slit Valve Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cruciform Slit Valve
Brand
Phoenix Biomedical
Lot Codes / Batch Numbers
UbaV/V020/07-2003
Products Sold
UbaV/V020/07-2003
Phoenix Biomedical is recalling Cruciform Slit Valve due to mislabeled - product actually Single Valve. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
mislabeled - product actually Single Valve
Recommended Action
Per FDA guidance
The recalling firm faxed copies of recall letters to the hospitals informing them of the problem and the need to return the product.
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 noticeDistribution
As reported by FDA
AZ, CA, IN
Page updated: Jan 10, 2026