Device Recall Remel Thayer Martin Agar (Improved)

  • Model / Serial
    10 pack - Lot #384341, Exp. 11/03/2003; 15 pack - Lot #384342, Exp. 11/3/2003; 100/cs - Lot #384343
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution was made nationwide to facilities with medical laboratories, including military and government facilities.
  • Product Description
    Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884), 15-packs (Cat. #01885), and 100 per case (Cat. #01886). The responsible firm on the label is Remel, Lenexa, KS.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Remel, Inc, 12076 Santa Fe Trail Dr, Lenexa KS 66215-3519
  • Source
    USFDA