Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens
Summary
The FDA issued a Class II for Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-6 by Immuno-Mycologics, Inc. Reason: Neutralization Buffer may contain contaminants.
Details
Source
Device Recall
External ID
Z-1984-2026
Action Date
2026-05-06
Status
Ongoing
Category
device
Product Description
Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens for Mycobacterium spp. diagnosis
Lot/Code Info: Lot: F5061154/UDI: 00816387021091
Quantity Affected: 101 units
Reason for Recall
Neutralization Buffer may contain contaminants
Distribution
US Nationwide distribution in the states of AZ, MS, SC, CT, NC, TX, IN, WA, MO, MI, CA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-26
Company
Norman, OK
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 275 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Immuno-Mycologics, Inc has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Immuno-Mycologics, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Immuno-Mycologics, Inc have FDA actions?
Immuno-Mycologics, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1984-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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