Devices

Device Recall Bemis

  • Model / Serial
    Lot #20040001 and Lot #20040004
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The recalled containers were shipped to consignees in Connecticut, Florida, Georgia, Pennsylvania and Tennessee in the United States, and to a consignee in Canada.
  • Product Description
    Bemis Two-Gallon Sharps Container, Models #102 020, #102 030, and #102 040. (The only difference between the models is in color. Model 102 040 is yellow, Model 102 020 is beige and Model 102 030 is red. )
  • Manufacturer
    Bemis Manufacturing Co.
  • 1 Event

Manufacturer

Bemis Manufacturing Co.
  • Manufacturer Address
    Bemis Manufacturing Co., Highway Pp West, Sheboygan Falls WI 53085
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Bemis/ Medline
  • Model / Serial
    BEMIS: Model 7H150 020 includes lot 20060001 to 20060016;  BEMiS: Model 7H150 030 includes lot 20050006, 20060001 to 20060008;  BEMIS: Model 7H150 040 includes lot 20060001 to 20060008;  Medline Model 7H950 030 includes lot 20050027, 20060001 to 20060008.
  • Product Classification
    General Hospital and Personal Use Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and Canada.
  • Product Description
    5 Qt. Wallmount Sharps Container, Model 150, Regular Size; colors 202 Beige, 030 Red, 040 Yellow, 24 count containers; Made in USA for: Medline Industries; BEMIS label has Manufactured by Bemis Mtg. Co., Sheboygan Falls, WI.
  • Manufacturer
    Bemis Health Care,Inc