FDA recall Z-3236-2017

NOVADAQ TECHNOLOGIES INC. · Class II · device

Product

NOVADAQ SPY-PHI Drape, 7" x 104" (18 cm x 265 cm), Ref. HH 2020 (box of 20 HH2000 drapes), Sterile, Rx.. Manufactured for: Novadaq Technologies Inc., Burnaby, BC, Canada. 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.

Reason for recall

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

Distribution

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

Key facts

Status
Terminated
Initiation date
2017-06-27
Report date
2017-10-04
Termination date
2017-12-11
Voluntary/Mandated
Voluntary: Firm initiated
Location
Burnaby, N/A, Canada

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3236-2017