FDA Enforcement Class II Terminated

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 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.

Recall: Z-3234-2017 · Reported October 4, 2017

Enforcement

Recall Number
Z-3234-2017
Event ID
77901
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
NOVADAQ TECHNOLOGIES INC.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
October 4, 2017
Initiation Date
June 27, 2017
Classification Date
September 28, 2017
Termination Date
December 11, 2017
Address
8329 Eastlake Dr Unit 101, N/A, Burnaby, N/A, N/A, Canada

Description

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 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

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

Code Info

Lot number 1704121

Distribution

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

Quantity

6 drapes