Medical device recalls Moderate risk

Ultradent Products, Inc. recalls Ultradent Products, Inc. Paper Points, Size 20 PN #1560, 200 per container, sterile. Product Usage: The product is used…

Recall date
August 4, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-3214-2017
FDA classification
Class II
Brand / firm
Ultradent Products, Inc.
Sold / distributed
Distribution was nationwide. Foreign distribution was made to Canada, Bulgaria, Namibia, New Zealand and Germany. There was no military /government distribution.

Why it was recalled

The barcode label was placed underneath the sterile barrier and the product was re-wrapped.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ultradent Products, Inc. Paper Points, Size 20 PN #1560, 200 per container, sterile. Product Usage: The product is used to assure that all moisture is removed from the root canal before the obturation procedure begins.

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