Product Safety Recalls

Product Recall Tracker

Microbiologics Inc Recall 89694

Description: Mycoplasma genitalium Control Panel (Inactivated Pellet)

Microbiologics Inc Recall 89694 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0784-2022
Event ID89694
Event DescriptionMycoplasma genitalium Control Panel (Inactivated Pellet)
Product TypeDevices
DistributionDistribution 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
Quantity80 units
Recall ReasonDistributed product did not undergo proper release testing.
Device Classification20220323
Device Code InfoCatalog 8240, Lots: 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 (UDI: 70845357043053)
Center Classification Date20220314
Recall Initiation Date20220225
Recalling FirmMicrobiologics Inc
Initial Notification E-Mail
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.