Data Foundry

Medical device recalls 2018

5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar — Class II medical device recall Z-1584-2018

Terminated recall by CooperSurgical, Inc., reported 2018-05-09, distributed nationwide. Products have been packaged with the wrong Trocar length type.

Recall numberZ-1584-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCooperSurgical, Inc., Trumbull, CT, United States
Recall initiated2018-03-12
Classified2018-05-01
Reported by FDA2018-05-09
Terminated2019-05-08
DistributedNationwide (US)
Countries outside the USAT, CA, CL, IT, SG
Quantity520 products
Lot numbers223333
Model numbers900-840

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 for recall

Products have been packaged with the wrong Trocar length type.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1584-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.