Medical device recalls Moderate risk

Terumo Medical Corporation recalls Terumo Needle, 18G x 1", Product Code NN1825R

Recall date
February 8, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2004-2019
FDA classification
Class II
Brand / firm
Terumo Medical Corporation
Sold / distributed
The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

Why it was recalled

There is a potential for a loss of package integrity that may compromise the sterility of the product.

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

What was recalled

Terumo Needle, 18G x 1", Product Code NN1825R

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