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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