NEXGEN Complete Knee Solution Monoblock Tibial Drill with stop 10 — Class II medical device recall Z-1376-2013
Terminated recall by Zimmer, Inc., reported 2013-06-05, distributed nationwide. Zimmer is initiating a lot specific recall of the Trabecular Metal" Tibia Stop Drill due to the potential of t
| Recall number | Z-1376-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2013-03-27 |
| Classified | 2013-05-24 |
| Reported by FDA | 2013-06-05 |
| Terminated | 2017-01-26 |
| Distributed | Nationwide (US) |
| Quantity | 69 units |
| Lot numbers | 62181290, 62183430 |
| Model numbers | 00-5887-052-00 |
Product
NEXGEN Complete Knee Solution Monoblock Tibial Drill with stop 10.7 mm. Used to prepare cylindrical holes in the native tibia.
Reason for recall
Zimmer is initiating a lot specific recall of the Trabecular Metal" Tibia Stop Drill due to the potential of the outside diameter being oversized. As a result, there is a potential for the drill to not pass through the applicable drill guide.
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-1376-2013. 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.