SX-One MicroKnife
Check against the official notice below — it lists the full affected range.
Sonex Health LLC is recalling 3,752 SX-One MicroKnife devices distributed nationwide across 28 states due to a potential dull blade hazard. The affected devices have Part Number 600112-001 and specific lot codes ranging from 20013120 to 41585.
The recall affects units distributed in Arizona, California, Colorado, Florida, Georgia, Hawaii, Idaho, Indiana, Kansas, Maryland, Michigan, Minnesota, Montana, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Texas, Utah, Virginia, Wisconsin, West Virginia, and Wyoming. The source does not specify a remedy for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Potential of dull blade
Reason for recall: Potential of dull blade Distribution: US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, ID, IN, KS, MD, MI, MN, MT, NE, NJ, NV, NY, OH, OK, OR, PA, TX, UT, VA, WI, WV, WY. Quantity: 3,752 devices Lot/code info: Part Number 600112-001; UDI-DI: 00860002094700; Lot Codes: 20013120, 20022821, 20022822, 20022823, 20022824, 20022825, 20070603, 20070604, 20080435, 20080436, 20083114, 20083115, 40051, 40052, 40472, 40473, 40892, 40893, 41460, 41584, 41585.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.