Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0036-2017Class II

Zenostar MT Color D4 60ml, art. no. 681065

Ivoclar Vivadent, Inc. / initiated 2016-05-27 / Terminated / root cause: manufacturing process

Ivoclar Vivadent, Inc. began a recall of Zenostar MT Color D4 60ml, art. no. 681065. Product Usage: For coloring dental porcelain on . FDA classified it as Class II and gives the reason as "The primary packaging of these products may show leaks in individual cases. As a consequence, the liquid may escape inadvertently and direct contact with this liquid may lead to skin irritation". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-0036-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Ivoclar Vivadent, Inc.
Product
Zenostar MT Color D4 60ml, art. no. 681065. Product Usage: For coloring dental porcelain
Product code
EIH Powder, Porcelain
Reason for recall
The primary packaging of these products may show leaks in individual cases. As a consequence, the liquid may escape inadvertently and direct contact with this liquid may lead to skin irritation.
Root cause tag
manufacturing process
FDA root cause
Process design
Action
Wieland sent an Urgent Medical Device Recall Notification letters dated May 27, 2016, and Response Forms to their customers via courier service to customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to Segregate any affected materials immediately. Customers were asked to complete the attached Acknowledgment form and return it to Ivoclar Vivadent, Inc. by mail, fax or email as indicated on the form. For questions contact Ivoclar Vivadent Technical Customer Service at 800-533-6825.
Quantity in commerce
9 units
Distribution
US Nationwide Distribution in the states of: AK, AL, AZ, CA, CO, CT, FL, IA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NY, OH, OR, PA, TN, TX, UT, VA, WA, and WI.
Product codes and lots
Lot No: U38680, exp date: Sep 15 2017

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-0036-2017
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-0017-2017Class IITerminatedVoluntary: Firm initiated
Z-0018-2017Class IITerminatedVoluntary: Firm initiated
Z-0019-2017Class IITerminatedVoluntary: Firm initiated
Z-0020-2017Class IITerminatedVoluntary: Firm initiated
Z-0021-2017Class IITerminatedVoluntary: Firm initiated
Z-0022-2017Class IITerminatedVoluntary: Firm initiated
Z-0023-2017Class IITerminatedVoluntary: Firm initiated
Z-0024-2017Class IITerminatedVoluntary: Firm initiated
Z-0025-2017Class IITerminatedVoluntary: Firm initiated
Z-0026-2017Class IITerminatedVoluntary: Firm initiated
Z-0027-2017Class IITerminatedVoluntary: Firm initiated
Z-0028-2017Class IITerminatedVoluntary: Firm initiated
Z-0029-2017Class IITerminatedVoluntary: Firm initiated
Z-0030-2017Class IITerminatedVoluntary: Firm initiated
Z-0031-2017Class IITerminatedVoluntary: Firm initiated
Z-0032-2017Class IITerminatedVoluntary: Firm initiated
Z-0033-2017Class IITerminatedVoluntary: Firm initiated
Z-0034-2017Class IITerminatedVoluntary: Firm initiated
Z-0035-2017Class IITerminatedVoluntary: Firm initiated
Z-0036-2017Class IITerminatedVoluntary: Firm initiated
Z-0037-2017Class IITerminatedVoluntary: Firm initiated