JAS Diagnostics Inc.: Medical Device Recall in 2014 - (Recall #: Z-1873-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum.

Product Classification:

Class II

Date Initiated: April 7, 2014

Date Posted: July 2, 2014

Recall Number: Z-1873-2014

Event ID: 68343

Reason for Recall:

JAS Diagnostics, Inc. of Miami Lakes, FL is recalling their Glucose Hexokinase reagent due to certain lots not performing according to their specifications.

Status: Terminated

Product Quantity: 407

Code Information:

LOTS#: N060208K, N060209K, N0602010K, N0902014K, N0902015K, N0902016K, N0902017K, N0902018K, N0902019K, N0902020K, N1102021K, N1102022K, N1102023K, N1102024K, N1102025K, N1102026K, N1102027K, N1102028K, N1102029K.

Distribution Pattern:

Worldwide Distribution - US including Puerto Rico and the states of CA, FL, TX, PA, GA, KY, MI, NY, OK, MN, TN, VA, NC, NV, NJ and WV, and the countries of Barbados, Ghana, Trinidad, Tobago, Canada and Haiti.

Voluntary or Mandated:

Voluntary: Firm initiated