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PATTERSON DENTAL SUPPLY, INC.

US Last updated 23 Oct 2026

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Devices
651
Registries
GUDIDFDA
FDA recalls
1

Catalogue651

Page 1 of 14

Showing 1-50 of 651

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2010

    • 15 Oct 2010 Z-0716-2011 Unclassified (pre-2012) Terminated Patterson Dental is conducting a recall because they have been advised by the manufacturer of Revolution Formula 2 (Kerr Corporation) that some syringes and tips marked with the brand name are not manufactured and distributed by Kerr and, thus, not authentic product.

Information

Country
US
Address
1031 MENDOTA HEIGHTS RD., ST. PAUL, MN, 55120
FDA FEI number
2183301