WhichRecall
Class IIReported 2026-01-21

Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 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

Recalled by Heraeus Medical GmbH (Dental Division)

Reason for Recall

increase of complaints regarding the breakage of the ampoules within their device systems

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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.

Recall Number
Z-1080-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-12-09
Reported
2026-01-21
Distribution
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.
Code Info
Lot Code: UDI-DI: 04260102136120; 04260102136151
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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