The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Recalled Product 

  • Product Name: Abacus Order Entry and Calculation Software
  • Product Codes: See medical device database entry
  • Devices Recalled in the U.S.: 9 (3 versions of software with 3 configurations)
  • Affected Customers: 1,114 
  • Dates