Recall Ledger

Immy recall (Immuno-Mycologics, Inc)

Medical deviceClass IIOngoing

Summary: Immuno-Mycologics, Inc is recalling Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis. Reason: Neutralization Buffer may contain contaminants.

What is being recalled

Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis

Why

Neutralization Buffer may contain contaminants

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide distribution in the states of AZ, MS, SC, CT, NC, TX, IN, WA, MO, MI, CA. (states named: Arizona, California, Connecticut, Indiana, Michigan, Missouri, Mississippi, North Carolina, South Carolina, Texas, Washington)

How to tell if yours is affected

Lot: F5061154/UDI: 00816387021091

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1984-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMarch 26, 2026
ReportedMay 6, 2026
CompanyImmuno-Mycologics, Inc
Company locationNorman, OK, United States
Initiated byVoluntary: Firm initiated
Quantity101 units

More recalls from Immuno-Mycologics, Inc · all medical device recalls · recalls from March 2026

Official FDA record