Medical device recalls Moderate risk

Centese Inc. recalls Thoraguard Chest Tube Kit, 20 Fr

Recall date
August 31, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0105-2022
FDA classification
Class II
Brand / firm
Centese Inc.
Sold / distributed
Distribution to a single consignee located in California.

Why it was recalled

An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Thoraguard Chest Tube Kit, 20 Fr

Get recall alerts

Free email alert whenever Centese Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Centese Inc.