SonoSite L25 Bracket Kit containing 1 Reusable non-sterile bracket recalled over sterility concerns
- Recall date
- November 2, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- CIVCO Medical Instruments Co., Inc. recalls SonoSite L25 Bracket Kit containing 1 Reusable non-sterile bracket, REF numbers P03122-01, P03122-02, P03122-03, P03122…
- Recall number
- Z-0563-2019
- FDA classification
- Class II
- Brand / firm
- CIVCO Medical Instruments Co., Inc.
- Sold / distributed
- Foreign distribution was made to Canada, Argentina, Australia, Austria, Belgium, Brazil, Chile, China, Colombia, Croatia, Cyprus, Denmark, Estonia, France, Germany, Hong Kong, India, Israel, Italy, Japan, Latvia, Lebanon, Lithuania, Netherlands, New Zealand, Philippines, Poland, Portugal, Qatar, Ro…
Why it was recalled
The needle guide bracket may puncture the sterile cover applied over the transducer and bracket during assembly.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
SonoSite L25 Bracket Kit containing 1 Reusable non-sterile bracket, REF numbers P03122-01, P03122-02, P03122-03, P03122-04, and P03122-05, Mfg for: SonoSite, Inc., Bothell, WA.
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