FDA recall Z-0265-2025

Beckman Coulter, Inc. · Class II · device

Product

Access Thyroglobulin Antibody II, REF A32898, containing Instructions for Use, IFU REF B14994, B63978, and A38168. The Access Thyroglobulin Antibody II (TgAb) assay is used for the quantitative determination of thyroglobulin antibody levels in human serum and plasma using the Access Immunoassay Systems.

Reason for recall

IFUs for the device incorrectly states the biotin interference was remediated. The issue could result in potentially false-low results.

Distribution

Distribution was made nationwide to the U.S., including Puerto Rico. There was government distribution but no military distribution. Foreign distribution was made to Mexico.

Key facts

Status
Ongoing
Initiation date
2024-09-05
Report date
2024-11-06
Voluntary/Mandated
Voluntary: Firm initiated
Location
Chaska, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0265-2025