FDA recall Z-0910-2023

Bayer Medical Care, Inc. · Class II · device

Product

Source Administration Set (SAS) used with the Medrad Intego PET Infusion System, Sterile Catalog number: INT CSS Affected material number: 86566621 Intended to deliver accurate doses of 18F Fluorodeoxyglucose (FDG) or 18F Sodium Fluoride (NaF) radiopharmaceuticals and commonly used flushing solutions to patients during molecular imaging (PET Positron Emission Tomography - nuclear medicine) diagnostic procedures.

Reason for recall

Black specks may be present on the packaged needles

Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, IN, MN, NY, OH, TX, VA and the country of China.

Key facts

Status
Ongoing
Initiation date
2022-11-30
Report date
2023-01-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Indianola, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0910-2023