FDA Device recall Z-1584-2018
5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count)
- FDA Device
- Class II
- terminated
- Published 2018-05-09
On 2018-05-09 the FDA classified a Class II recall of 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count) by Coopersurgical, citing products have been packaged with the wrong Trocar length type.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1584-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-12 |
| Published | 2018-05-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Coopersurgical |
| Distribution | US |
Product
5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage: The Apple-Hunt Secondary Cannulas are indicated for use in laparoscopic surgical procedures to provide a pathway for the introduction of endoscopic surgical instruments and allow for maintenance of pneumoperitoneum. For uninhibited laparoscopic access, the Apple-Hunt Cannula/Trocar provides greater instrument maneuverability while maintaining an airtight seal -with no bulky external valves, fittings, or housings. The ergonomic trocar design is simple to use and features a smooth cannula/trocar transition for easier sleeve insertion and reduced risk of patient injury.
Reason
Products have been packaged with the wrong Trocar length type.
Identifiers
| code_info | Lot number 223333 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1584-2018%22
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