The Recall Desk
ModerateFDA (Devices)·Z-0028-2017·Announced 2016-10-12

Ivoclar Vivadent Recalls Zenostar MT Color B3 Dental Porcelain Liquid

Ivoclar Vivadent is recalling 27 units of Zenostar MT Color B3 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity score. The hazard involves potential skin irritation from liquid leakage, which is a low-risk contamination issue without reports of serious injury or hospitalization.

Plain-English summary

Ivoclar Vivadent, Inc. is recalling 27 units of Zenostar MT Color B3 60ml dental porcelain liquid, article number 681057. The affected product is identified by Lot No. U38751 and has an expiration date of September 15, 2017.

The recall is being issued because 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.

The product was distributed nationwide in the United States, specifically 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. Consumers and dental professionals should stop using the affected product and contact the recalling firm for instructions on return or disposal.

The recalled product

Product
Zenostar MT Color B3 60ml, art. no. 681057. Product Usage: For coloring dental porcelain
Manufacturer
Ivoclar Vivadent, Inc.
Category
Medical Device — Dental Materials
Hazard
Affected units
27

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • Lot No: U38751
  • exp date: Sep 15 2017

Distribution

Distributed nationwide across the United States.

The notice also names 31 states specifically:

Part of a larger recall action

This product is one of 21 recalled by Ivoclar Vivadent, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 21 products in this recall →

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