Bard Access Systems: 13 recalls on record

Recalls filed with 1 agency: FDA (13).

First recall on record: September 5, 2012. Most recent: January 18, 2017.

Risk classification: Class II: 11 · Class III: 2

Most recent recalls

DateAgencyProduct
January 18, 2017FDASafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as si…Z-0986-2017
January 18, 2017FDAMiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code: S02022-75. Pa…Z-0985-2017
January 18, 2017FDAStatLock¿ CV Plus w/Pigtail. Product Code: CV0220CE & CV0220. Packaged as a single unit w…Z-0982-2017
January 18, 2017FDAStatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Packaged as a single …Z-0981-2017
July 15, 2015FDAPowerPICC SOLO Catheter with Tip Location System (TLS) Stylet 4F Nurse Full Tray with Mic…Z-2049-2015
December 10, 2014FDAGuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer: Bard Access…Z-0493-2015
April 2, 2014FDAPowerPort Slim Implantable Port, indicated for patient therapies requiring repeated acces…Z-1300-2014
January 29, 2014FDAMRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Catheter. Product Code 0…Z-0814-2014
January 29, 2014FDATitanium Single Lumen Low-Profile port, with Pre-Attached open-Ended Silicone 6.6Fr Cathe…Z-0815-2014
July 10, 2013FDAStatLock CV Plus w/Pigtail, Catheter Stabilization Device Sterile EO Single Use Only, C.R…Z-1618-2013
March 13, 2013FDAHickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart…Z-0909-2013
March 13, 2013FDALeonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apar…Z-0910-2013
September 5, 2012FDA16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an A…Z-2277-2012

Questions about this company

How many recalls does Bard Access Systems have?
Recalert has 13 U.S. recalls on record for Bard Access Systems, published between September 5, 2012 and January 18, 2017.
What was the most recent Bard Access Systems recall?
FDA recall Z-0986-2017, published January 18, 2017: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: …
Which agencies have handled Bard Access Systems recalls?
Bard Access Systems appears as the recalling firm in recalls from: FDA (13).

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