KWIK-STIK, Quality control kit for culture media, Vibrio ... (Microbiologics Inc) – some products packaged for lot 818-11... (2025)
Product mislabeling can potentially compromise quality control procedures.
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, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Brand
Microbiologics Inc
Lot Codes / Batch Numbers
UDI-DI: 30845357020018, Lot Number: 818-111-7
Products Sold
UDI-DI: 30845357020018; Lot Number: 818-111-7
Microbiologics Inc is recalling KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, C due to Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Recommended Action
Per FDA guidance
An Urgent Medical Device Recall notification letter dated 11/13/25 was sent to customers. INSTRUCTIONS: 1.CONTACT END USERS who have received or may have received the affected items above and provide them with the Customer Communication and Customer Response Forms. 2.COMPLETE the Distributor Response Form provided. 3.RETURN the response forms to recall@microbiologics.com. 4.KEEP this letter for your records. 5.CONTACT Microbiologics if a replacement kit is needed. Microbiologics is dedicated to ensuring the success of your quality control processes. Please contact our Recall Support team at 320.229.7080 or recall@microbiologics.com with questions or concerns. Collect calls may be made.
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