FDA Recall Terminated

KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.

Recall: Z-0511-2022 · Initiated December 16, 2020

Recall

Recall Number
Z-0511-2022
Event Number
89285
Firm
Microbiologics Inc
FEI Number
2150138
Product Code
JTR
Status
Terminated
Root Cause
Material/Component Contamination
Initiated
December 16, 2020
Terminated
July 7, 2022
Address
200 Cooper Ave N, Saint Cloud, MN, 56303-4440

Description

KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.

Reason

Contamination with S. epidermidis

Action

The recalling firm issued letters beginning 12/16/2020 to their consignees explaining the reason for recall and that due to the distinct morphology of Microsporum canis, it is possible to distinguish between the 2 colonies and select the correct microorganism from an agar plate for testing. The consignee was provided the instructions to review their lab procedures to understand how this information affects their usage, use or discard depending on their lab procedures and how this information affects their usage, complete the response form and return it to the firm. The letter is to kept for their records and the firm is to be contacted for a replacement kit if needed. The response form was to indicate the consignee has acknowledged receipt of the information, has updated their records, and to report the number of kits on hand. If the consignee has discarded or destroyed individual units, they are to indicate the quantity needed for replacement.

Distribution

Distribution was made to CA, IA, IL, LA, MA, MI, NY, PA, SD, TN, VA, WI, and WV. There was no government/military distribution. Foreign distribution was made to Brazil, Canada, Colombia, Dominican Republic, Finland, France, India, Japan, Malaysia, Mexico, Netherlands, Poland, Romania, Saudi Arabia, Serbia, South Africa, and United Kingdom.

Quantity

59 kits