Retractable Technologies, Inc. recalls EasyPoint Needle, 25G x 5/8", REF: 82091
- Recall date
- February 5, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1293-2024
- FDA classification
- Class II
- Brand / firm
- Retractable Technologies, Inc.
- Sold / distributed
- US Nationwide distribution including in the states of NY, FL, IL, MA, UT, NJ, AZ, MO, WA, NC, CA, TX, NV, IN, PA, VA, IA, GA, TN, MI, OH, OK, CO, OR, SC, MN, CT.
Why it was recalled
The needle cannula of a retractable needle may detach from the needle holder in the patient.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
EasyPoint Needle, 25G x 5/8", REF: 82091
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