Data Foundry

Medical device recalls 2017

Drill Bit Quick-Connect 2 — Class II medical device recall Z-3193-2017

Terminated recall by Zimmer Biomet, Inc., reported 2017-10-04, distributed nationwide. Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with

Recall numberZ-3193-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Biomet, Inc., Warsaw, IN, United States
Recall initiated2017-05-22
Classified2017-09-22
Reported by FDA2017-10-04
Terminated2019-03-29
DistributedNationwide (US)
Countries outside the USAU, BR, CA, CN, DE, GT, IN, JP, KR, MX, MY, NL, PA, SG, SV, TT, TW
Quantity2,585 units
Reason classesdevice malfunction
Lot numbers63398778, 63426469, 63431693, 63431763, 63444579, 63444581, 63444582, 63444584, 63444587, 63451645, 63451647, 63451648, 63451649, 63451651, 63451655, 63462151, 63462166, 63462170, 63462174, 63474142, 63478948, 63484963, 63484966, 63484973, 63492362, 63492363, 63505347, 63505348, 63510772, 63510773, 63524431, 63545255, 63562124, 63566199, 63566218, 63584030
Model numbers00480610020

Product

Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length, Item Number/EDI 00480610020, Nonsterile. orthopedic surgical instrument.

Reason for recall

Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. The anomaly may be on or below the surface and can increase the risk of instrument fracture.

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-3193-2017. 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.