Recall Z-0583-2022

Microbiologics Inc · initiated October 1, 2020

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

LYFO DISK(TM), LYFO DISK(TM) Streptococcus pneumoniae derived from ATCC(R) 49619(TM). LYFO DISK microorganisms are packaged in a resealable vial that contains 6 lyophilized microorganism pellets and a desiccant to prevent adverse moisture accumulation. The LYFO DISK microorganisms are 3 passages or fewer from the reference culture and are guaranteed to recover when processed using the recommended media and incubation requirements.

Codes / lots: Catalog Number: 0947L, Lot Number: 947-126-1, UDI: 10845357022964

Reason for recall

Potential contamination with Escherichia coli, Staphylococcus epidermidis and S. warneri.

FDA-determined cause: Unknown/Undetermined by firm

Action taken

Microbiologics notified customers on about 10/01/2020 via letter titled "Urgent Medical Device Recall." Instructions included to inspect inventory for affected products. If found, instructions included the following: 1. REVIEW lab procedures to understand how this information affects your usage; 2. USE OR DISCARD depending on your lab procedures and how this information affects your usage; 3. COMPLETE the response form provided; 4. RETURN the response form to recall@microbiologics.com; 5. KEEP this letter for your records; 6. CONTACT Microbiologics if a replacement kit is needed. Questions or concerns can be directed to Recall Support team at 320.229.7073 or recall@microbiologics.com.

Details

Recall number
Z-0583-2022
Initiated
October 1, 2020
Terminated
July 7, 2022
Product code
JTR – Kit, Quality Control For Culture Media
Quantity
42 units
Distribution
Worldwide distribution - US Nationwide distribution in the states of AR, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MS, MT, NC, ND, NE, NM, NY, OH, OK, OR, PR, SC, TN, TX, VA, VT, WA, WV and the countries of AUSTRALIA, AUSTRIA, BAHRAIN, BELARUS, BELGIUM, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, FRANCE, GEORGIA, GERMANY, GUATAMALA, HONG KONG, INDIA, INDONESIA, IRELAND, ITALY…
Recalling firm
Microbiologics Inc, Saint Cloud, MN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0582-2022 Class IIKWIK-STIK(TM), Streptococcus pneumoniae derived from ATCC(R) 49619(TM), packaged as…Potential contamination with S. epidermidis E. coli and S. warneri. 10/01/2020Terminated
Z-0584-2022 Class IIQC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive…Potential contamination with Escherichia coli Staphylococcus epidermidis and S. warneri. 10/01/2020Terminated