IBA Dosimetry Lift Table Recalled for Uncontrolled Movement Risk

Plain-English summary

IBA Dosimetry GmbH is recalling Lift Table Type 4320 units, identified by catalog numbers HA03-010#2 and HA03-000#2. The recall covers specific serial numbers listed in the official FDA record. These devices were distributed nationwide and internationally to various countries, including the United States, Germany, France, and Italy.

The recall is being issued because, in very rare occasions, the electric lift table may start to move up in an uncontrolled manner when connected to the mains power. This uncontrolled movement presents a potential safety hazard to users and patients in the vicinity of the device.

Users of these devices should stop using the affected lift tables immediately and contact IBA Dosimetry GmbH for instructions on how to proceed with the recall. The company is responsible for managing the corrective actions associated with this recall.

The recalled product

Product

IBA Dosimetry GmbH Lift Table Type 4320, Catalog HA03-010#2 and HA03-000#2

Manufacturer

Iba Dosimetry Gmbh

Category

Medical Device — Radiation Therapy Equipment

Hazard

• uncontrolled-movement

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Distribution

Related recalls