FDA recall Z-0519-2024

Meridian Bioscience Inc · Class II · device

Product

Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312

Reason for recall

Plastic vials contain a manufacturing defect may cause an increased risk of leakage and presents a risk of incidental exposure to biological hazards associated with direct contact with the patient specimen.

Distribution

Nationwide Foreign: Italy

Key facts

Status
Ongoing
Initiation date
2023-10-19
Report date
2023-12-20
Voluntary/Mandated
Voluntary: Firm initiated
Location
Cincinnati, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0519-2024