Z-1474-2026Class II

Remel, Inc

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm

Remel, Inc

Product type

Device

Status

Ongoing

Report date

2026-03-04

Distribution

US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.

Firm state

Product quantity

Initiated by

Voluntary: Firm initiated

Reason for recall

Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

Product description

Campy CVA Medium 100/PK, R01272

Code / lot info

UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →