Diagnostica Stago, Inc. STA-Compact Hemostasis System with Cap piercing capability. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
STA-Compact Hemostasis System with Cap piercing capability.
Brand
Diagnostica Stago, Inc.
Lot Codes / Batch Numbers
All distributed units with cap piecing option.
Products Sold
All distributed units with cap piecing option.
Diagnostica Stago, Inc. is recalling STA-Compact Hemostasis System with Cap piercing capability. due to With maintenance of the STA line, the cap-piercing feature may involve potential risk of needle puncture injury.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
With maintenance of the STA line, the cap-piercing feature may involve potential risk of needle puncture injury.
Recommended Action
Per FDA guidance
The firm sent out letters on March 5, 2003 to their customers alerting them to the problem and providing further guidance on how to prevent the problem. The firm will be sending out to the customers a protective device to attach to the needle assembly as soon as possible
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