Cardinal Health 200, LLC recalls Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
- Recall date
- April 30, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2048-2019
- FDA classification
- Class II
- Brand / firm
- Cardinal Health 200, LLC
- Sold / distributed
- Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL
Why it was recalled
Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier 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
Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314
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