FDA recall Z-1520-2021

Oto Med Inc · Class II · device

Product

Grace Medical REF S-3500 *** COX BONE DUST COLLECTOR *** 2 stainless steel filters - Product Usage: intended to be inserted into a suction tube during the early stages of otologic surgery to collect bone particles for future use.

Reason for recall

During internal Age Testing, holes were found in the sterile Tyvek pouches of the devices.

Distribution

Worldwide distribution - U.S. Nationwide distribution including in the states of MN, IL, PA, WI, GA, SD, FL, AR, MA, AZ, TX, MO, NC, CA, UT, DE, OR, IN, CO, AL, OH, NY, WA, DC, TN, NH, VT, VA, SC, MI, WI, MS, IA, NJ, MD, KS, CT, LA, ME, KY, HI, TN, RI, NV, ID and the countries of Argentina, Brazil, Colombia, Chile, Hong Kong, South Africa, United Arab Emirates, Taiwan, Canada, India.

Key facts

Status
Ongoing
Initiation date
2020-12-07
Report date
2021-05-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Havasu City, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1520-2021