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Month: January 2019

Pro-Med Instruments Recalls the DORO LUCENT Headrest Due to Possible Malfunction and Failure

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Name: DORO® LUCENT Base Unit, Locking Transitional Member, and Transitional Member Serial numbers: 1704001, 1704042, 1709001, 1709096 Manufacturing Dates: May 4, 2017 to April 5, 2018 Distribution Dates: Marc...
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Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product(s): Synaptive Medical, Inc. BrightMatter Guide with SurfaceTrace Registration Model/Product Numbers: SYN-0026 (Versions: 1.5.0, 1.5.1 and 1.5.2) Manufacturing Dates: November 17, 2017 to April 24, 2018 Distri...
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