Device Recall Bard PEG

  • Model / Serial
    Lots: 43FQAO78, 43FQA186, 43GQA080, 43HQA083, 43lQA092, 43JQA083,43KQA197, 43LQA202, HURA1457, HURB2555, HURD1301, HURD1995, HURE2973, HURE3447, HURE3448, HURF0572, HURG0273, HURH0036, HURH1222, HURJ0797, HURK1562, HUSA0504, HUSB1435, HUSC0155, HUSD0380, HUSD2072, HUSE0001, HUSF0580.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Canada, Australia, and Japan.
  • Product Description
    Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire" REF 003030, 20F, Sterile.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    C.R. Bard Access Systems, Inc, 5425 Amelia Earhart Dr, Salt Lake City UT 84116-3713
  • Source
    USFDA

2 devices with a similar name

Learn more about the data here

  • Model / Serial
    Lots: 43FQA076, 43IQA096, 43KQA098, HURD1299, HURE3445 , HURI0365, HUSA0502, HUSC0154.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Canada, Australia, and Japan.
  • Product Description
    Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire" , REF 003028, 28F, Sterile.
  • Manufacturer
  • Model / Serial
    Lots: 43DQA032 , 43FQA161, 43GQA068, 43HQA056, 43IQA058, 43JQA059, 43KQA075, 43LQA078, HURA1477, HURB2561, HURD0513, HURD1835, HURE2826, HURF0409, HURG1390, HURH0876, HURJ0544, HURJ0545, HURJ1447, HURJ1448, HUSD0101, HUSD1943, HUSE1509, HUSF1754.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide, including USA, Belgium, Canada, Australia, and Japan.
  • Product Description
    Bard Access Systems, Inc., Bard* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Guidewire", REF 006036, 20F, Sterile.
  • Manufacturer