[Recalled] Radiography 7300 C; Model Number: 712037; — Philips has identified that some ceiling suspension telescopic carriages manufa… | FDA 2025-10-01

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

This Class II recall concerns device products distributed in Germany and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Philips Medical Systems DMC GmbH

• DigitalDiagnost 4 High Performance. radiography and fluoroscopy system — Class II
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• ProxiDiagnost N90. radiography and fluoroscopy system — Class II
• Precision CRF; Model Number: 706400; — Class II
• DigitalDiagnost C90 High Performance. radiography and fluoroscopy system — Class II
• DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.