RegWardenFDA facility compliance records
Facility

Kerr Corporation

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2013: 1 recalls; 2015: 1 recalls1’13’141’15’16’17’18’19’20’21’22’23’24’25’26
  • Recalls (2)

Devices registered here (1)

  • Adhesive, Bracket And Tooth Conditioner, Resin
    Product code DYH (opens in a new tab) · Class II · Dental · 21 CFR 872.3750

Recalls & enforcement

  • Class IITerminated2015-02-11
    Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips, have inner boxes labeled with part number 4500 which fit 7mm and 8mm tips. There is a low risk associated with the use of the product as the sleeve may tear causing a potential for cross contamination.
  • Class IITerminated2013-06-06
    The firm initiated the recall of AOA Mini RPE Screw Assembly, because it may be missing a complete weld joining one side of the arm with the screw body. Herbst, MARA and Fixed Metal devices may be affected, because they contain an AOA Mini RPE Screw Assembly.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Kerr Corporation (FEI 2024312) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2024312-kerr-corporation/

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