NOVADAQ TECHNOLOGIES INC.: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: December 3, 2014. Most recent: October 4, 2017.
Risk classification: Class II: 3 · Class III: 2
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| October 4, 2017 | FDA | NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH2000 (single drape), Sterile, …Z-3234-2017 | Z-3234-2017 |
| October 4, 2017 | FDA | NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System, Product Code HH9006, contai…Z-3235-2017 | Z-3235-2017 |
| March 9, 2016 | FDA | PINPOINT Endoscopic Fluorescence Imaging SystemZ-1032-2016 | Z-1032-2016 |
| December 3, 2014 | FDA | Non-sterile drapeZ-0470-2015 | Z-0470-2015 |
| December 3, 2014 | FDA | LUNA Chest, Model No. LU4006Z-0469-2015 | Z-0469-2015 |
Questions about this company
- How many recalls does NOVADAQ TECHNOLOGIES INC. have?
- Recalert has 5 U.S. recalls on record for NOVADAQ TECHNOLOGIES INC., published between December 3, 2014 and October 4, 2017.
- What was the most recent NOVADAQ TECHNOLOGIES INC. recall?
- FDA recall Z-3234-2017, published October 4, 2017: NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH2000 (single drape), Sterile, Rx. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. The SPY-PHI Drape is intended to co…
- Which agencies have handled NOVADAQ TECHNOLOGIES INC. recalls?
- NOVADAQ TECHNOLOGIES INC. appears as the recalling firm in recalls from: FDA (5).
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