Voco Recalls
4 recalls on record · January 18, 2017 to February 28, 2024 · Medical Devices
Recalls by year
17
19
24
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 28, 2024Medical DevicesFDA
Voco GmbH recalls Ionolux, Catalog (REF) Numbers: a) 2115, b)2117, c) 2118, d) 2119, e) 2120, f) 2122; dental cement
Hazard: Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for Ionolux. When these capsules are activated, curing is significantly delayed and incomplete. Processing according to the instructions for use is not possible.
February 28, 2024Medical DevicesFDA
Voco GmbH recalls IonoStar Plus, Catalog (REF) Numbers: a) 2540, b)2543, c) 2544, d) 2545, e) 2546, f) 2547, g) 2549; dental cement
Hazard: Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for Ionolux. When these capsules are activated, curing is significantly delayed and incomplete. Processing according to the instructions for use is not possible.
October 9, 2019Medical DevicesFDA
Voco GmbH recalls Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling small
Hazard: The metal cannula are potentially too loose and may become loose when applying the filing material.
January 18, 2017Medical DevicesFDA
Voco GmbH recalls VOCO Futurabond M+ adhesive, RF 1515, Manufactured by VOCO GmbH, Futurabond M+ is a dental adhesive for use with methacr
Hazard: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled as Futurabond M+ Universal Adhesive.