Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:13490
Brand Name:Ethicon Absorbable SPIRALOK Anchor with Absorbable Suture
Model:222960, 222962, 222986, 222988
Affected:All lots
Software version:
Recalling Organisation:Johnson & Johnson (NZ) Limited
13a Gabador Place
Mt Wellington
AUCKLAND 1060
Contact Information:0800 922 638
Manufacturer:DePuy Mitek
Brand Name:Ethicon Absorbable SPIRALOK Anchor with Non absorbable Suture
Model:222961, 222963, 222965
Affected:All lots
Software version:
Recalling Organisation:Johnson & Johnson (NZ) Limited
13a Gabador Place
Mt Wellington
AUCKLAND 1060
Contact Information:0800 922 638
Manufacturer:DePuy Mitek
Brand Name:Ethicon Absorbable SPIRALOK Anchor with Needles
Model:222985, 222987
Affected:All lots
Software version:
Recalling Organisation:Johnson & Johnson (NZ) Limited
13a Gabador Place
Mt Wellington
AUCKLAND 1060
Contact Information:0800 922 638
Manufacturer:DePuy Mitek
Issue:Based on internal testing and post market clinical information the manufacturer has determined that SPIRALOK Anchors may not be as robust compared to other similarly indicated anchors offered today. Spiralok anchors are being withdrawn from the market.
Recall action type:Recall
Recall action:Product to be returned to supplier
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:12/9/2012
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