FDA Recall
Terminated
Site-Rite Sterile Needle Guide Kit - 20 gauge
Recall: Z-0715-05
·
Initiated November 3, 2004
Recall
- Recall Number
- Z-0715-05
- Event Number
- 30396
- Firm
- Bard Access Systems, Inc
- FEI Number
- 3006260740
- Product Code
- ITX
- Status
- Terminated
- Root Cause
- Other
- Initiated
- November 3, 2004
- Posted
- April 22, 2005
- Terminated
- April 22, 2005
- Address
- 5425 Amelia Earhart Dr, Salt Lake City, UT, 84116-3713
Description
Site-Rite Sterile Needle Guide Kit - 20 gauge
Reason
Conductivity gel pouches, labeled as sterile, and packaged in various needle guide kits may not be sterile.
Action
All domestic consignees were notified by letter on 10/04/2004. All foreign consignees were notified by letter on 10/15/04.
Distribution
Nationwide. Foreign distribution to: Austria; Bahrain, Belgium, Bermuda, Brazil, Canada, Greece, Hong Kong, Italy, Japan, Kuwait, Malaysia, Mexico, Norway, Oman, Pakistan, Portugal, Qatar, Saudi Arabia, Switzerland, Turkey, United Arab Emirates, United Kingdom.
Quantity
34,619 units