Medical device recalls Moderate risk

COVIDIEN LLC recalls Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both prima…

Recall date
August 1, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0015-2019
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

Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

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