Baxter Corporation Englewood recalls Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93…

Recall date

December 29, 2014

Source

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

Recall number

Z-1227-2015

FDA classification

Class II

Brand / firm

Baxter Corporation Englewood

Sold / distributed

Nationwide Distribution

Why it was recalled

Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.

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

What was recalled

Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.