The Recall Desk
SevereFDA (Devices)·Z-0712-2013·Announced 2013-01-30

DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class II and involves a structural defect in a spinal implant where the screw shank may separate, posing a significant risk of injury.

Plain-English summary

DePuy Spine, Inc. is recalling 6 units of VIPER Polyaxial Screws (Product Code: 1867-15-180). The recall covers the 5.5 10 X 80MM Tl model, which is a spinal implant component.

The recall was initiated because polyaxial screws 8x 80 and larger may disassociate when inserted in the Ilium. Specifically, in high-torque circumstances, the screw shank has the potential to separate from the polyaxial head.

The affected units were distributed worldwide, including nationwide in the United States (specifically AZ, CA, FL, HI, IL, MD, MI, MO, NC, TN, TX) and in Australia. All lots are affected. Healthcare providers should contact DePuy Spine for further instructions on handling these devices.

The recalled product

Product
DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Product Code: 1867-15-180 Spinal Implant Component.
Manufacturer
DePuy Spine, Inc.
Affected units
6

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • All lots

Distribution

Distributed nationwide across the United States.

The notice also names 11 states specifically:

Part of a larger recall action

This product is one of 9 recalled by DePuy Spine, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 9 products in this recall →