Device Recall PrepStain Syringing Pipettes

  • Model / Serial
    100901a, 100902f, 100902f, 100903d, 100908c, 100910c, 100914f, 100916d, 100921d, 100928c, 101005a, 101007d, 101008c, 101012c, 101013a, 101015c, 101020d, 101022c, 101027a, 101028c, 101029d, 101103b, 101105h, 101110f, 101111c, 101117p, 101118n,  101119c, 101130p, 101201o, 101207o, 101208p, 101210c, 101213n, 101214b, 101214c,  101217b, 101220q, 101221g, 110104b, 110106a, 110107c, 110110d, 110112n, 110118b,  110128i, 110203i, 110210r
  • Product Classification
  • Device Class
    3
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution.
  • Product Description
    PrepStain Syringing Pipettes 240 (Catalog #490517)
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Tripath Imaging, Inc., 780 Plantation Dr, Burlington NC 27215-6723
  • Manufacturer Parent Company (2017)
  • Source
    USFDA