FDA Device recall Z-2315-2015
Aequalis Humeral Nail Targeting Jig, Product Code: 9020060
- FDA Device
- Class II
- terminated
- Published 2015-08-05
On 2015-08-05 the FDA classified a Class II recall of Aequalis Humeral Nail Targeting Jig, Product Code: 9020060 by Tornier, citing 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 ji….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2315-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-06-25 |
| Published | 2015-08-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Tornier |
| Distribution | AK, AL, AZ, CA, CO, CT, FL, IL, IN, MD, ME, MI, MO, NC, OH, PA, TX |
Product
Aequalis Humeral Nail Targeting Jig, Product Code: 9020060. Orthopedic manual surgical instrument.
Reason
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.
Identifiers
| code_info | Lots: DB0114069, DB0114349, CA46096, CA216052, DB0111264001, DB0112016, DB0113102. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2315-2015%22
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