Arrow International Inc recalls Epidural Needle; Product Codes: AN-05501 and AN-05505
- Recall date
- April 11, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1961-2018
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- US Nationwide, AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CZECH REPUBLIC, DENMARK, ECUADOR, FRANCE, GERMANY, GREECE, HONG KONG, INDONESIA, IRELAND, ITALY, JAPAN, KOREA, NETHERLANDS, NEW ZEALAND, PANAMA, PHILIPPINES, POLAND, PUERTO RICO, ROMANIA, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, SPAIN, SWE…
Why it was recalled
Product sterility may be compromised due to unsealed packaging.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Epidural Needle; Product Codes: AN-05501 and AN-05505
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