Bard Access Systems, Inc.
Bard Access Systems, Inc.: 3 recalls listed since July 2026 across FDA; 2 rated high risk.
By year
- 20263
By agency
- FDA3
By category
- Medical Device3
All recalls (3)
Bard Access Systems DuoGlide and Power-Trialysis Short-Term Straight Dialysis Catheter
Bard Access Systems is recalling its Power-Trialysis Short-Term Straight Dialysis Catheter because this is a downstream recall of class I recall RES 98777.
2 products
Bard Access Systems BD Needle Kit for Powered Driver
BD Needle Kit for Powered Driver may have difficulty removing the obturator, potentially delaying therapy and causing serious injury or death.
Bard Catheters, Dialysis Catheters, and Biopsy Trays
The lidocaine ampoules in these devices were manufactured under deficient practices and are being recalled by the supplier.
14 products