Resource Optimization & Innovation LLC recalls Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site
- Recall date
- February 28, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0950-2022
- FDA classification
- Class II
- Brand / firm
- Resource Optimization & Innovation LLC
- Sold / distributed
- US distribution to two consignees located in Missouri
Why it was recalled
A kit component, the PDI Prevantics Swab, was recalled.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site
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