Summary
The FDA issued a Class II for SX-One MicroKnife by SONEX HEALTH LLC. Reason: Potential of dull blade.
Details
Source
Device Recall
External ID
Z-1387-2022
Action Date
2022-07-27
Status
Terminated
Category
device
Product Description
SX-One MicroKnife
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.
Quantity Affected: 3,752 devices
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-29
Company
Eagan, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 176 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SONEX HEALTH LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SONEX HEALTH LLC have FDA actions?
This is the only FDA action we have on record for SONEX HEALTH LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1387-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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