Diagnostic Hybrids Inc: Medical Device Recall in 2013 - (Recall #: Z-0792-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplification of viruses, such as respiratory viruses, enteroviruses, measles, and poliovirus from patient specimens.

Product Classification:

Class III

Date Initiated: December 31, 2012

Date Posted: February 13, 2013

Recall Number: Z-0792-2013

Event ID: 64115

Reason for Recall:

RhMK product fungal contamination.

Status: Terminated

Product Quantity: 13,005 units

Code Information:

Model #:49-0600, Lot#, 491206T, 491216; Model #: 49-0600A, Lot#, -A-491206T, -A-491216, -A-491216B; Model #: 49-0102A, Lot#, -A-491206T, -A-491216 and Model #: 49-T075A, Lot#, -A-491206T, -A-491216.

Distribution Pattern:

Nationwide Distribution including the states of AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA & WI.

Voluntary or Mandated:

Voluntary: Firm initiated