FDA Recall Terminated

Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.

Recall: Z-1089-2019 · Initiated March 1, 2019

Recall

Recall Number
Z-1089-2019
Event Number
82361
Firm
Integra Limited
FEI Number
3001700044
Product Code
HWC
Status
Terminated
Root Cause
Process control
Initiated
March 1, 2019
Terminated
June 22, 2020
Address
311 Enterprise Dr, Plainsboro, NJ, 08536-3344

Description

Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.

Reason

Temperature indicator may have changed color to dark gray or black prior to shipment. Change in color may indicate the product exposure to temperatures greater than 110F

Action

Integra LifeSciences Corp. notified consignees (Hospitals and Distributors) by letter delivered by courier service, facsimile or email about the initial notification on March 1st, 2019.Letter explains problem, health risk and action to take: examine inventory to determine if you have any affected lots with discolored temperature dots, where the dots look similar as pictures labeled UNACCEPTABLE on previous page.. If you do have any product with discolored temperature dots, stop using the product immediately, remove them from service and place in quarantine until the product can be returned. Complete the attached Acknowledgement and Return Form. Questions Customer Service at 1-800-654-2873 Monday to Friday 8:00 AM 8:00 PM EST or [email protected] .

Distribution

US Nationwide distribution in the states of OH, MI.

Quantity

232 total