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Recall Observatory FDA recall evidence

Device product

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.

Z-0792-2013

December 31, 2012

Class III

Product summary

Firm
Diagnostic Hybrids Inc
Event
Event 64115
Status
Terminated
Classification
Class III
Quantity
13,005 units
Official record key
device-enforcement:Z-0792-2013

Official wording

Reason: RhMK product fungal contamination.

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.

Derived failure modes

  • Microbial contamination

    reason.microbial_contamination · v1.0.0

    fungal contamination