KWIK-STIK Clostridium (Microbiologics) – Labeling Error (2022)
This recall involves a labeling issue.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
KWIK-STIK" plus: Clostridium perfringens
Brand
Microbiologics Inc
Lot Codes / Batch Numbers
catalog number: 0801P, lot number: 801-44-4, expiration date: 05/31/2023, UDI: 20845357019374
Products Sold
catalog number: 0801P; lot number: 801-44-4; expiration date: 05/31/2023; UDI: 20845357019374
Microbiologics Inc is recalling KWIK-STIK" plus: Clostridium perfringens due to Labeling error.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Labeling error.
Recommended Action
Per FDA guidance
The firm issued a recall notification to the consignees beginning on 05/06/2022 via email. The letter informs the consignee to inspect inventory, review lab procedures, use or discard affected product depending on lab procedures, and complete the response form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026