Microbiologics Inc: Medical Device Recall in 2025 - (Recall #: Z-1957-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K, Staphylococcus aureus derived from NCTC 12493

Product Classification:

Class II

Date Initiated: May 27, 2025

Date Posted: June 18, 2025

Recall Number: Z-1957-2025

Event ID: 96974

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.

Status: Ongoing

Product Quantity: 3 total

Code Information:

01065K: UDI-DI 30845357032868, lot 1065-25-51; 0621K: UDI-DI 30845357014666, lot 621-73-21

Distribution Pattern:

US Nationwide distribution in the states of California and Pennsylvania and the country of New Zealand.

Voluntary or Mandated:

Voluntary: Firm initiated