FDA Media Alert Detail

Device Recall

FDA Device Recall: Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594,...

  • U.S. Food and Drug Administration
  • September 2, 2026
  • ID: device-Z-3016-2026

Device Enforcement Report Details

Recall NumberZ-3016-2026
Recalling FirmHenry Schein Inc.
ClassificationClass II
Voluntary / MandatedVoluntary: Firm initiated
Distribution PatternWorldwide distribution - US Nationwide and the country of Barbados.
StatusOngoing
Device ClassN/A
Device NameN/A
Product Description

Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm, Product Codes: 1) 949-3594, Mfr Product Code 1840; Lots 2529604, 2538147, 2608145 2) 949-3595, Mfr Product Code 1841; Lots 2539075, 2539313, 2609789, 2539065 3) 949-3596, Mfr Product Code 1842; Lots 2536632, 2609174, 2610099 4) 949-3597, Mfr Product Code 1843; Lots 2535296, 2537418, 2607283 is a light-cured, nano-hybrid dental composite restorative material intended for direct restorative procedures.

Reason for Recall

Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

Code Information

Product Codes: 1) 949-3594, Mfr Product Code 1840, Lot Numbers: 2529604, 2538147, 2608145; 2) 949-3595, Mfr Product Code 1841, Lot Numbers: 2539075, 2539313, 2609789, 2539065; 3) 949-3596, Mfr Product Code 1842, Lot Numbers: 2536632, 2609174, 2610099; 4) 949-3597, Mfr Product Code 1843, Lot Numbers: 2535296, 2537418, 2607283.


Content syndicated from the U.S. Food and Drug Administration (FDA) device enforcement reports database.