FDA Device recall Z-1846-2016
Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive and open surgical pro…
- FDA Device
- Class II
- terminated
- Published 2016-06-08
On 2016-06-08 the FDA classified a Class II recall of Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive and open surgical pro… by Sterilmed, citing sterlilmed is recalling all unexpired Scissor Tips because of a potential manufacturing defect that can possibly result in a patient injury.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1846-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-04-26 |
| Published | 2016-06-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Sterilmed |
| Distribution | AL, AR, CA, CO, FL, GA, IA, IN, KY, MA, MD, MI, MN, MO, NC, NJ, NV, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV |
Product
Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive and open surgical procedures to facilitate cutting, preparation, mobilization, and coagulation of tissue. Model #'s MIC3112, MIC3122, MIC3132, MIC3142, MIC3152, MIC3162.
Reason
Sterlilmed is recalling all unexpired Scissor Tips because of a potential manufacturing defect that can possibly result in a patient injury.
Identifiers
| code_info | Lot Number MIC3112 / 1850033 1851382 1852899 1853678 1855660 1856511 1856900 1859438 1859965 1860367 186156…Lot Number MIC3112 / 1850033 1851382 1852899 1853678 1855660 1856511 1856900 1859438 1859965 1860367 1861563 1862954 1863647 1864260 1865162 1865993 1867015 1867706 1868934 1870036 1870103 1871206 1872270 1873830 1874518 1875721 1876911 1878327 1879082 1880420 1880667 1880964 1882288 1883924 1884996 1886199 1886912 1887725 1889721 1889771 1890036 1890089 1891061 1891534 1891745 1892678 1893796 1893818 1893872 1894880 1895807 1896467 1897219 1898693 1899180 1900106 1901160 1901950 1903029 1903645 1904549 1905627 1906345 1907168 1907920 1908583 1909201 1910229 1911281 1912196 1912496 1913274 1913316 1914703 MIC3122/ 1850033 1851382 1856511 1856900 1859438 1861563 1868934 1870103 1872882 1875721 1878327 1879082 1896467 1897219 1898693 1899795 1900106 1901160 1903029 1905604 1906345 1907168 1910229 1911281 1912196 MIC3132 / 1850033 1851382 1852883 1852899 1853678 1854157 1856900 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1846-2016%22
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