Data Foundry

Medical device recalls 2015

Aequalis Humeral Nail Targeting Jig — Class II medical device recall Z-2315-2015

Terminated recall by Tornier, Inc, reported 2015-08-05, distributed in AK, AL, AZ, CA, CO, CT, FL, IL…. Recall for the Aequalis IM Nail instrumentation set (Tray Number 9020000) due to several reports that the mast

Recall numberZ-2315-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTornier, Inc, Bloomington, MN, United States
Recall initiated2015-06-25
Classified2015-07-29
Reported by FDA2015-08-05
Terminated2017-08-31
DistributedAK, AL, AZ, CA, CO, CT, FL, IL, IN, MD, ME, MI, MO, NC, OH, PA, TX
Countries outside the USCA, FR
Quantity99
Lot numbersCA216052, CA46096, DB0111264001, DB0112016, DB0113102, DB0114069, DB0114349

Product

Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.

Reason for recall

Recall for the Aequalis IM Nail instrumentation set (Tray Number 9020000) due to several reports that the mast of the targeting jig (Part Number 9020060) is separating from the jig boom. Separation will impact alignment and can affect the ability to fixate Aequalis IM Nail screws.

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-2315-2015. 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.