FDA recall Z-0485-2024

Atrium Medical Corporation · Class II · device

Product

Atrium Oasis Dry Suction Water Seal Chest Drain, Part Number: 3600-100, DRAIN, OASIS SINGLE W/AC, 3600 SINGLE COLLECTION.

Reason for recall

Product was re-processed and re-sterilized by a third party using packaging configurations and a sterilization process which are not approved by the manufacture and lack validation.

Distribution

US: VA

Key facts

Status
Ongoing
Initiation date
2023-09-05
Report date
2023-12-13
Voluntary/Mandated
Voluntary: Firm initiated
Location
Merrimack, NH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0485-2024