FDA Device recall Z-1435-2019
Drill, cannulated, 4x120mm, AO, Item Number 502015402
- FDA Device
- Class II
- terminated
- Published 2019-05-29
On 2019-05-29 the FDA classified a Class II recall of Drill, cannulated, 4x120mm, AO, Item Number 502015402 by Zimmer, citing an investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1435-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-04-08 |
| Published | 2019-05-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer |
| Distribution | AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, WY |
Product
Drill, cannulated, 4x120mm, AO, Item Number 502015402
Reason
An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications.
Identifiers
| code_info | All items marked with "Normed" are affected |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1435-2019%22
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