Cadence Inc. recalls Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
- Recall date
- July 9, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2364-2015
- 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
Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
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