FDA recall Z-1001-2022

Sight Sciences, Inc. · Class II · device

Product

TearCare version 1.0 SmartHubs

Reason for recall

Ophthalmic devices distributed prior to the recently-obtained 510(k) clearance do not fall within the relevant 510(k) exemption and so their performance characteristics were not evaluated by the FDA prior to distribution.

Distribution

US Nationwide distribution in the states of PA, CA, OH, AZ, CT, NC, GA, TN, MS, RI, WA, IL, FL, NV, NE, VA, SD, KY, OK, NJ, CO, TX, MI, NY, AR, WI, OR, MO, AL, NM, UT, WV, SC, IN, KS, MA, MN, NH, MT, ND, MD, WY, HI, DC, ID, LA, DE.

Key facts

Status
Ongoing
Initiation date
2022-03-23
Report date
2022-05-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Menlo Park, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1001-2022