The Recall Desk
ModerateFDA (Devices)·Z-2991-2017·Announced 2017-08-16

Valorem Surgical Recalls Pallas M Compass Spinal Fixation Devices

Valorem Surgical LLC is recalling 262 Pallas M/MAXIMIS Compass devices because they are not consistent with Quality System Requirements.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the source text cites non-compliance with Quality System Requirements without reporting specific injuries, illnesses, or deaths, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Valorem Surgical LLC is recalling 262 units of the Pallas M/MAXIMIS Compass, which is part of the MAXIMIS Pedicle Screw Spinal Fixation System. The devices are intended for posterior pedicle screw fixation of the non-cervical spine. The recall is being conducted because the devices are not consistent with Quality System Requirements.

The affected products were distributed nationwide in the United States, including California and Virginia. The specific catalog number is 0902-1019, and the known lot numbers are WNV120816 and WNV111108. The product was labeled as the Pallas M Spinal Fixation System through 2015.

Healthcare providers and consumers should check their inventory for these specific lot numbers and contact Valorem Surgical LLC for further instructions on how to handle the recalled devices.

The recalled product

Product
PALLAS M/MAXIMIS Compass. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
Manufacturer
Valorem Surgical LLC
Category
Medical Device — Orthopedic / Spinal Fixation
Hazard
Affected units
262

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 (3)

  • Catalog No. 0902-1019
  • Known Lot No. WNV120816
  • WNV111108.

Distribution

Distributed nationwide across the United States.

The notice also names 2 states specifically:

Part of a larger recall action

This product is one of 144 recalled by Valorem Surgical LLC 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 144 products in this recall →

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