Remel, Inc: Medical Device Recall in 2025 - (Recall #: Z-1200-2025)

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:

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

Product Classification:

Class II

Date Initiated: February 13, 2025

Date Posted: February 26, 2025

Recall Number: Z-1200-2025

Event ID: 96312

Reason for Recall:

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Status: Ongoing

Product Quantity: 787 units

Code Information:

UDI/DI 848838003691, Lot Number 213926, exp. 2025-02-24

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated