FDA recall record

Microbiologics KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus recall — FDA Z-0876-2026

Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.

Class IIclassification
Z-0876-2026official record ID
Dec 10, 2025report date

Recall record at a glance

Official recordZ-0876-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMicrobiologics Inc.
Report dateDec 10, 2025
Recall initiation dateNov 13, 2025
Quantity5 units
LocationSaint Cloud, MN, United States

Official product description

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Why the product was recalled

Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.

Distribution information

International distribution to the countries of UAE, China, Singapore, Kazakhstan,

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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