Centurion Medical Products Corporation recalls DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for g…
- Recall date
- July 1, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2167-2019
- FDA classification
- Class II
- Brand / firm
- Centurion Medical Products Corporation
- Sold / distributed
- US Nationwide distribution in the states of AZ, CA, FL, GA, IL, KY, MA, MD, MI, NC, NH, NY, OH, SC, TX, TN, VA, WA, WI.
Why it was recalled
Potential for sterile packaging to be compromised
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DAILY DRIVELINE KIT Kit Code: DM940 - Product Usage: Kit is used for Driveline Maintenance and Securement of Line for general patient population.
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