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NOVADAQ TECHNOLOGIES Recalls
7 recalls on record · December 3, 2014 to October 4, 2017 · Medical Devices
Recalls by year
14
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 4, 2017Medical DevicesFDA
NOVADAQ TECHNOLOGIES INC. recalls NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured fo
Hazard: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
October 4, 2017Medical DevicesFDA
NOVADAQ TECHNOLOGIES INC. recalls NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System, Product Code HH9006, containing 6 Single-Procedure Kits (P
Hazard: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
October 4, 2017Medical DevicesFDA
NOVADAQ TECHNOLOGIES INC. recalls NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH2000 (single drape), Sterile, Rx. Manufactured for: Novadaq
Hazard: The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier.
September 14, 2016Medical DevicesFDA
NOVADAQ TECHNOLOGIES INC. recalls Sterile Drape, SK6000 PAQ drape pouch (for use with the SPY Fluorescent System (SPY 2000/2001)) The SPY Fluorescent I
Hazard: Novadaq is informing SK6000 PAQ users that a pinhole through the drape pouch film material was identified in some SK6000 PAQs during shipping validation testing.
March 9, 2016Medical DevicesFDA
Novadaq Technologies Inc. recalls PINPOINT Endoscopic Fluorescence Imaging System
Hazard: It has been determined that the PINPOINT Operator's Manual does not contain validated parameters for gravity-cycle autoclave sterilization of the PINPOINT laparoscopes and light guide cable in the reprocessing tray.
December 3, 2014Medical DevicesFDA
Novadaq Technologies, Inc. recalls Non-sterile drape
Hazard: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional contents sterile label.
December 3, 2014Medical DevicesFDA
Novadaq Technologies, Inc. recalls LUNA Chest, Model No. LU4006
Hazard: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional contents sterile label.