RecallRadar

FDA Device recall Z-1584-2018

5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count)

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

AgencyFDA Device
Recall numberZ-1584-2018
ClassificationClass II
Statusterminated
Initiated2018-03-12
Published2018-05-09
Last updated2026-09-13 11:54 UTC
CompanyCoopersurgical
DistributionUS

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_infoLot 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

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.