Micro-Mate Tuberculin Glass Syringe recalled over sterility concerns
- Recall date
- July 9, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Cadence Inc. recalls Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
- Recall number
- Z-2365-2015
- FDA classification
- Class II
- Brand / firm
- Cadence Inc.
- Sold / distributed
- Nationwide Foreign Canada, Denmark. Italy
Why it was recalled
Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
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