Arrow International Inc recalls Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
- Recall date
- December 20, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1239-2020
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Why it was recalled
Product lidstock contains the incorrect expiration date for 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
Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
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