Remel, Inc: Medical Device Recall in 2025 - (Recall #: Z-0585-2026)

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:

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

Product Classification:

Class II

Date Initiated: November 12, 2025

Date Posted: December 3, 2025

Recall Number: Z-0585-2026

Event ID: 97967

Reason for Recall:

Products may contain contamination, which may result in a darker or brown media color.

Status: Ongoing

Product Quantity: 1,000 US, 280 ROW

Code Information:

1. UDI-DI 848838018831, lots 305529, 311228, 316019, 320993 2. UDI-DI 848838091353, lot 317287

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AK, CA, FL, GA, IA, IL, IN, LA, MA, MD, ME, MI, MN, NE, NY, OH, OK, PA, RI, SD, TN, VA, WA, WI and the countries of Brazil, Canada, China, Cyprus, Finland, Great Britain, Ireland, Moldova, Norway, Singapore.

Voluntary or Mandated:

Voluntary: Firm initiated