Medical device recalls Moderate risk

COVIDIEN LLC recalls Dermacea Gauze Fluff Roll, 6 Ply, 4 x 4-1/8 yd (10.2 cm x 3.7 m), REF 441106 Product Usage: Used as both primary and se…

Recall date
August 1, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0018-2019
FDA classification
Class II
Brand / firm
COVIDIEN LLC
Sold / distributed
US Nationwide Distribution

Why it was recalled

Potential for product sterility breach due to a compromised or pinched seal defect

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

What was recalled

Dermacea Gauze Fluff Roll, 6 Ply, 4 x 4-1/8 yd (10.2 cm x 3.7 m), REF 441106 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

Get recall alerts

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

More recalls from: COVIDIEN LLC