Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product fungal contamination.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Diagnostic Hybrids Inc directly.
Affected Products
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.
Quantity: 13,005 units
Why Was This Recalled?
RhMK product fungal contamination.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Diagnostic Hybrids Inc
Diagnostic Hybrids Inc has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report