FDAJuly 31, 2014device

Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800220161, 459800232931, 459800235871, 459800338451. UPDATED: Pinnacle3 Software Version 8.0h, 8.0k, 8.0m, 8.0n.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Philips, Pinnacle Radiation Treatment Planning System version 8.0h, 8.0k, 8.0m, 8.0n, 9 0, 9 2 9 4, 9 6 is being recalled because the dose may be inconsistent with the density of a density-overridden ROl.

What to do

FDA enforcement status: Terminated

Brands named

philips electronics north americaphilipsphilips electronics

UPCs

453560446041459800091001459800220161459800232931459800235871459800338451453560446051459800096361453560446061459800096541453560446091459800096741

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800220161, 459800232931, 459800235871, 459800338451. UPDATED: Pinnacle3 Software Version 8.0h, 8.0k, 8.0m, 8.0n. — Recall Details · AllClear