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FDA Medical Device Recalls (openFDA)

Microbiologics Inc: LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L

Recall number
Z-2195-2025
Recalling firm
Microbiologics Inc
Product
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L
Status
Open, Classified
Initiated
2025-06-27
Posted
2025-07-29
Terminated
not on file
Reason
KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.
Root cause
Under Investigation by firm
Action
Microbiologics issued an Urgent Medical Device Recall notice on 06/27/2025 via email. The notice explained the problem with the device, potential risk, and requested the following: INSTRUCTIONS: 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. NOTIFY other facilities or customers to whom the product may have been distributed or transferred. 7. CONTACT Microbiologics if a replacement kit is needed. Contact Recall Support team at 320.229.7080 or recall@microbiologics.com with questions or concerns.
Quantity
not on file
Distribution
Worldwide distribution - US Nationwide and the countries of France, Colombia, Philippines, Peru, Turkey, India, Finland, Trinidad and Tobago, Poland, Viet Nam, Brazil, Japan, Malaysia, Costa Rica.
Lot, serial or model codes
1) 0894L: UDI/DI 10845357021967, Lot Numbers 894-76-4 and 894-76-6
510(k) numbers
not on file
PMA numbers
not on file
Product code
JTR
Firm FEI
2150138
Firm city
Saint Cloud
Firm state
MN
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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