Novadaq Technologies, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0470-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Non-sterile drape

Product Classification:

Class III

Date Initiated: November 4, 2014

Date Posted: December 3, 2014

Recall Number: Z-0470-2015

Event ID: 69839

Reason for Recall:

Non sterile-drape LUNA drape was inadvertently mislabeled with an additional contents sterile label.

Status: Terminated

Product Quantity: 324 units

Code Information:

Kit Lot Numbers: 14082, 14091, 14104, 14106 Drape Lot Numbers: D132712, D133102, D141022, D130282

Distribution Pattern:

Nationwide Distribution to IA, LA, GA, MD, ID, FL, TN, OH, TX, NC, MA, KY, KS, WI, IN, SC, OR, CT, CA, WA, PA, OK, and PR.

Voluntary or Mandated:

Voluntary: Firm initiated