Covidien LLC recalls Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for…

Recall date

August 6, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2525-2015

FDA classification

Class II

Brand / firm

Covidien LLC

Sold / distributed

US Nationwide Distribution

Why it was recalled

Sterility may be compromised

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

What was recalled

Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.