RecallDepth

Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon to apply a recommended tension to the band and hold it in place during spine manipulation and set screw tightening.

Company
Orthopediatrics Corp
Recall Initiated
April 24, 2017
Terminated
September 18, 2017
Recall Number
Z-2321-2017
Quantity
82
Firm Location
Warsaw, IN

Reason for Recall

Over-tensioning of the band resulting in damage to the band causing it to rupture

Distribution

Worldwide Distribution-US distribution to: MO, NY, KY, FL, NC and OH; and countries of: AUSTRALIA, FRANCE and SPAIN.

Lot / Code Info

All lots Product Number: 01-1102-1000

Root Cause

Device Design

Action Taken

The firm, OrthoPediatrics Corp., contacted each distributor/consignee via phone on 4/24/2017, regarding the recall. The phone call informed Consignees of issue and actions to be taken. The consignees were instructed to return of devices in their control were issued; cease further distribution of the product and quarantine it. The firm state that product will be distributed after Rework to new revision. If you have any questions, contact V.P. Regulatory Affairs, at (574) 268-6379 or email: mfox@orthopediatrics.com.

More recalls by Orthopediatrics Corp

View all recalls by this company →