Devices

Device Recall Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump

Manufacturer

Stryker Instruments Div. of Stryker Corporation
  • Manufacturer Address
    Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump
  • Model / Serial
    Lot Numbers: 8136753340 through 9131936639.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- Including the United States, Argentina, Australia, Brazil, Canada, England, France, Germany, Hong Kong, Italy, Japan, Latin America, Malaysia, Mexico, Netherlands, New Zealand, Singapore, South Africa, Spain, Sweden, Switzerland and Taiwan.
  • Product Description
    Stryker 5.0 catheter set for PainPump2 and AutoFuser PainPump, sterile, Stryker Instruments, Kalamazoo, MI; REF 0537-005-000.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation