Remel, Inc: Medical Device Recall in 2025 - (Recall #: Z-2223-2025)

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:

Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

Product Classification:

Class II

Date Initiated: July 11, 2025

Date Posted: August 6, 2025

Recall Number: Z-2223-2025

Event ID: 97224

Reason for Recall:

The products may contain surface and subsurface contamination of Listeria monocytogenes.

Status: Ongoing

Product Quantity: 1552 units

Code Information:

UDI-DI: 848838000645; Lot Numbers: 271595, 271596

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated