Philips Medical Systems (Cleveland) Inc recalls Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems
- Recall date
- March 17, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2205-2015
- FDA classification
- Class II
- Brand / firm
- Philips Medical Systems (Cleveland) Inc
- Sold / distributed
- Worldwide Distribution-Product was shipped to the following states: AR, AR, AZ, CA, CO, CT, FL, GA, IA, IN, KS, LA, MA, MD, MI, MO, MS, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, VA, VT, WA, WV & WY, and to the following countries: Argentina, Australia, Bangladesh, Belgium, Brazil, Bulgaria, China…
Why it was recalled
A head holder released for use with other CT systems but not yet qualified for use on the Ingenuity CT, which was shipped with this system.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems
Get recall alerts
Free email alert whenever Philips Medical Systems (Cleveland) Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Philips Medical Systems (Cleveland) Inc