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Recall Observatory FDA recall evidence

Device product

NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System, Product Code HH9006, containing 6 Single-Procedure Kits (Product Code HH9001), each containing the sterile drape (HH2000), as well as single-use drug components, Manufactured for and Distributed by Novadaq Technologies Inc., Burnaby, BC, Canada, Assembled by Carestream Health, Inc., Rochester, NY. The SPY-PHI Drape is intended to cover the SPY-PHI System to maintain a sterile field, and as an aid in the clean-up of equipment after surgery or other medical procedures. The product is not intended to be used as patient drapes and they have no patient contact.

Z-3235-2017

June 27, 2017

Class II

Product summary

Firm
NOVADAQ TECHNOLOGIES INC.
Event
Event 77901
Status
Terminated
Classification
Class II
Quantity
16/6-drape kits
Official record key
device-enforcement:Z-3235-2017

Official wording

Reason: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.

Code information: PAQ lot #1704B containing drape lot #1703251; PAQ lot #1704F containing drape lot #1703291; and PAQ lot #17046 containing drape lot #1703251.

Distribution pattern: Worldwide Distribution. US (nationwide) to states of: CA, CO, ID, IL, NY, OR, and VA; and countries of: Canada, Belgium, and Lithuania.

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    breach of the sterile barrier