FDAFDA · Food and drugs·Recall number Z-0784-2022
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Published March 23, 2022 · Recall initiated: February 25, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Distributed product did not undergo proper release testing.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Microbiologics Inc
- Distributor
- Distribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA OUS distribution to Belgium, Finland, France, Germany, Ireland, Sweden, United Kingdom, and Vietnam
- Lot
- Catalog 8240, Lots: 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 (UDI: 70845357043053)
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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