CooperSurgical recalls 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar (Model 90: 223333) due to incorrect packaging. This may cause improper surgical use. Affected users should contact CooperSurgical for details.
Products have been packaged with the wrong Trocar length type.
CooperSurgical is recalling 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar (Model 900-840) because it was packaged with the wrong trocar length. This could lead to improper surgical use during laparoscopic procedures.
The recalled trocars were packaged with the wrong length, which could lead to improper surgical use. This might cause issues with instrument maneuverability or pneumoperitoneum maintenance during laparoscopic procedures.
Surgical professionals using the 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar (Model 900-840) for laparoscopic procedures are affected. Patients undergoing surgery with this device are at risk if the wrong length is used.
Check for the model number 900-840 on the packaging. The product was sold with lot number 223333. This specific trocar is used in laparoscopic surgery for introducing surgical instruments.
Reach out to CooperSurgical directly for details about the recall and next steps.
The product was packaged with the wrong trocar length, which could lead to improper surgical use during laparoscopic procedures.
Model number 900-840 (lot number 223333).
Check the packaging for model number 900-840 and lot number 223333. This trocar is used in laparoscopic surgery.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1584-2018 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-1584-2018 from CooperSurgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
