FDA Enforcement Class II Terminated

BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm. The BMC RF Cannula is sealed in a Tyvek pouch (primary packaging) and then placed into a white shelf-box (secondary packaging) with the instructions for use. A predetermined number of white shelf-boxes are then placed into shipping cartons (tertiary packaging). The BMC RF Cannula is intended for use in radiofrequency heat lesion procedures for relief of pain.

Recall: Z-0879-2013 · Reported March 6, 2013

Enforcement

Recall Number
Z-0879-2013
Event ID
64250
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Baylis Medical Company Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 6, 2013
Initiation Date
October 4, 2012
Classification Date
February 26, 2013
Termination Date
May 23, 2013
Address
5160 Explorer Drive #33, N/A, Mississauga, Ontario, N/A, Canada

Description

BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm. The BMC RF Cannula is sealed in a Tyvek pouch (primary packaging) and then placed into a white shelf-box (secondary packaging) with the instructions for use. A predetermined number of white shelf-boxes are then placed into shipping cartons (tertiary packaging). The BMC RF Cannula is intended for use in radiofrequency heat lesion procedures for relief of pain.

Reason

A report of an event was received indicating that upon opening a box containing 10 sterile cannula by a nurse, the pouch package of 5 of the 10 individually packaged cannula had not been sealed along one edge. Thus the pouch was open and the device could fall out of the pouch and on to the floor when retrieved from the shelf box. The cannulas were not used on any patients, as the unsealed packages

Code Info

Device Model #: 1 PMF 16-145-10CS. Lot number: PFFB 190811.

Distribution

International distribution to the country of Australia.

Quantity

1780