Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:21410
Brand Name:Suture unit, automatic
Model:
Affected:PolysorbTM Braided Absorbable Suture, EndoStitchTM Loading Unit with PolysorbTM Suture
Software version:
Recalling Organisation:Covidien NZ Ltd
Level 3, Building 5, Central Park Corporate Centre
666 Great South Road
Penrose
AUCKLAND 1051
Contact Information:0508 489 264
Manufacturer:Covidien LLC
Issue:Due to the potential for an incomplete seal on the inner package which may result in premature degradation of the suture material.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:8/5/2017
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