Medical device recalls Moderate risk

Arrow International Inc recalls Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes

Recall date
August 27, 2015
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2825-2015
FDA classification
Class II
Brand / firm
Arrow International Inc
Sold / distributed
Nationwide and internationally.

Why it was recalled

Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to compromised sterility of the outer barrel, Arrow purchased recalled items that were packaged with certain products.

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

What was recalled

Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes

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