Class II
Medical Device Recall: KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K, Staphylococcus aureus derived from NCTC 12493
Microbiologics Inc · May 27, 2025
Reason for Recall
Affected products were packaged with the incorrect KWIK STIK assembly resulting in the product containing the wrong microorganism. 0621K was packaged 01065K swabs; 01065K was packaged with 0621K swabs. This may lead to delayed diagnosis.
Distribution
US Nationwide distribution in the states of California and Pennsylvania and the country of New Zealand.
States Affected
NATIONWIDE
Quantity Affected
3 total
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1957-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.