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TL 5000/3000 – Surgical Light
Baxter Medical Systems GmbH + Co. KG · Model 4038130 · UDI-DI 00887761968424
10
510(k) clearances
17
Adverse events (2 deaths)
1
Recalls
28
Facilities
Description
TruLight 5000 / 3000 Wall
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-06-05 | Brainlab AG | Target Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for Leksell headrings a |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.