Recall Z-1443-2015— Bard Access Systems
Class II · Terminated
Class II FDA medical device recall by Bard Access Systems, initiated 2014-06-24, terminated 2015-11-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.. Reason: Potential for inadvertent scalpel stick injury involving the safety scalpel..
- Recalling firm
- Bard Access Systems
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-06-24
- Terminated
- 2015-11-05
- Firm location
- Salt Lake City, UT, United States
Product description
Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.
Reason for recall
Potential for inadvertent scalpel stick injury involving the safety scalpel.
Data sourced from openFDA. This site is unofficial and independent of the FDA.