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 number | Z-2662-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Exactech, Inc., Gainesville, FL, United States |
| Recall initiated | 2017-05-25 |
| Classified | 2017-07-03 |
| Reported by FDA | 2017-07-12 |
| Terminated | 2019-07-26 |
| Distributed | AL, 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 US | AU, CH, DE, ES, FR, GB, IN, IT, JP, KR, LU, NL, SG |
| Quantity | 573 |
| Reason classes | labeling, device malfunction |
| Lot numbers | 37166-002, 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 numbers | 213-75-01 |
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
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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.