Heraeus Medical GmbH (Dental Division): Device Recall

Recall #Z-1082-2026 · 12/09/2025

Class II: Risk

Recall Details

Recall Number
Z-1082-2026
Classification
Class II
Product Type
Device
Recalling Firm
Heraeus Medical GmbH (Dental Division)
Status
Ongoing
Date Initiated
12/09/2025
Location
Wehrheim, Germany
Voluntary/Mandated
Voluntary: Firm initiated

Reason for Recall

increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.

Product Description

Brand Name: PALACOS Product Name: PALACOS MV+G pro 40; PALACOS MV+G pro 80 Model/Catalog Number: 5081290; 5081291 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A

Distribution Pattern

International distribution in the countries of Aland Islands, Australia, Belgium, Denmark, Finland, Germany, Ireland, Italy, Liechtenstein, Netherlands, New Zealand, Norway, Portugal, Spain, Sweden, Switzerland, United Kingdom.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.