Recall Z-1690-2020

Microbiologics Inc · initiated February 12, 2020

Class II Terminated

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

Product

KWIK-STIK 2 Pack Trichosporon dermatis derived from ATCC 204094 (Catalog# 0778P, lot 778-65-3)

Codes / lots: Catalog Number: 0778P. Lot Number: 778-65-3. UDI 20845357018773.

Reason for recall

KWIKSTIK 2 Pack (REF 0778P) and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set (REF 5195P) contain product labeled as Trichosporon dermatis (T. dermatis) which may contain Candida Utilis instead of T. dermatis.

FDA-determined cause: Nonconforming Material/Component

Action taken

Microbiologics notified customer on 02/12/2020 via "Urgent Medical Device Correction" letter. The recall letter was emailed to consignees and the consignees were instructed to properly discard any affected products they have. The recall letter identified the affected product and lot numbers. Reason for the correction was also noted in the recall letter.

Details

Recall number
Z-1690-2020
Initiated
February 12, 2020
Terminated
March 26, 2021
Product code
JTR – Kit, Quality Control For Culture Media
Quantity
49 units
Distribution
Nationwide, Including Australia, Brazil, Curacao, Ecuador, Germany, Greece, Italy, Puerto Rico, Singapore, Turkey, United States, Uruguay and Australia.
Recalling firm
Microbiologics Inc, Saint Cloud, MN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1691-2020 Class IIMicrobiologics QC SETS AND PANELS, YST Comprehensive QC Set, REF 5195P, containing…KWIKSTIK 2 Pack (REF 0778P) and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set (REF 5195P) contain… 02/12/2020Terminated