FDA Device recall Z-2071-2017
Stryker PROFESS Registration Kit
- FDA Device
- Class II
- terminated
- Published 2017-05-17
On 2017-05-17 the FDA classified a Class II recall of Stryker PROFESS Registration Kit by Stryker Instruments Div, citing product shipped proximate to or past the expiration date listed on the product label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2071-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-10 |
| Published | 2017-05-17 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Instruments Div |
| Distribution | US |
Product
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guidance system to enable intranasal and sinus computer-assisted surgery. The system is comprised of PROFESS Registration Stickers, a PROFESS Patient Tracker, and a PROFESS Adaptor Cable.
Reason
Product shipped proximate to or past the expiration date listed on the product label.
Identifiers
| code_info | Lot #202085 Stryker Product Number: 6001-420-000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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All Stryker Instruments Div recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2071-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.