Data Foundry

Medical device recalls 2017

Logic Fit Tibial Tamp Head — Class II medical device recall Z-2662-2017

Terminated recall by Exactech, Inc., reported 2017-07-12, distributed in AL, AZ, CA, CO, FL, GA, HI, IA…. The firm determined that the labeling (surgical technique) should be updated to clarify the proper technique a

Recall numberZ-2662-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmExactech, Inc., Gainesville, FL, United States
Recall initiated2017-05-25
Classified2017-07-03
Reported by FDA2017-07-12
Terminated2019-07-26
DistributedAL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, LA, MA, MD, ME, MN, NC, NJ, NV, NY, OH, OK, OR, PR, RI, SC, TN, TX, VA, WA, WI
Countries outside the USAU, CH, DE, ES, FR, GB, IN, IT, JP, KR, LU, NL, SG
Quantity573
Reason classeslabeling, device malfunction
Lot numbers37166-002, 44944-004, 44944-005, 44944-006, 48073-010, 48073-011, 48073-012, 49036-017, 51180-004, 51180-005, 51180-006, 51180-008, 51754-031, 51754-032, 51754-033, 51754-034, 59743-001, 61872-001, 61872-002
Model numbers213-75-01

Product

Logic Fit Tibial Tamp Head

Reason for recall

The firm determined that the labeling (surgical technique) should be updated to clarify the proper technique and instrumentation to remove the tamp assembly from the bone, i.e., to include a caution statement about the potential for instrument breakage if the tamp handle/guide is misused by impacting in retro-grade.

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-2662-2017. 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.