Microbiologics Inc: Medical Device Recall in 2025 - (Recall #: Z-2124-2025)

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-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L

Product Classification:

Class II

Date Initiated: June 17, 2025

Date Posted: July 23, 2025

Recall Number: Z-2124-2025

Event ID: 97096

Reason for Recall:

Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.

Status: Ongoing

Product Quantity: 21 total

Code Information:

Lot #: 805-234-4, 805-234-5 UDI: (0805K) 30845357019531, (0805L) 10845357019544

Distribution Pattern:

US distribution to states of: Utah and Ohio; and OUS (International) to countries of: Italy, Netherlands, Argentina, Korea, Jordan, Spain, and Bangladesh.

Voluntary or Mandated:

Voluntary: Firm initiated