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