Data Foundry

Medical device recalls 2016

Reprocessed Microline Scissor Tips intended to be used with a… — Class II medical device recall Z-1846-2016

Terminated recall by STERILMED, INC., reported 2016-06-08, distributed in AL, AR, CA, CO, FL, GA, IA, IN…. Sterlilmed is recalling all unexpired Scissor Tips because of a potential manufacturing defect that can possib

Recall numberZ-1846-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSTERILMED, INC., Maple Grove, MN, United States
Recall initiated2016-04-26
Classified2016-05-31
Reported by FDA2016-06-08
Terminated2017-04-05
DistributedAL, 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
Countries outside the USCA
Quantity11,326
Lot numbers1850033, 1851382, 1852859, 1852883, 1852899, 1852905, 1853678, 1853937, 1854157, 1855660, 1855815, 1856511, 1856900, 1859438, 1859745, 1859965, 1860193, 1860367, 1861563, 1862228, 1862954, 1863647, 1864094, 1864260, 1865162, 1865902, 1865993, 1867015, 1867706, 1868934, 1869589, 1870036, 1870103, 1871206, 1872270, 1872882, 1873830, 1874518, 1874798, 1874852 and 75 more
Model numbersMIC3112, MIC3122, MIC3132, MIC3142, MIC3152, MIC3162

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 for recall

Sterlilmed is recalling all unexpired Scissor Tips because of a potential manufacturing defect that can possibly result in a patient injury.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1846-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.