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ADAC Laboratories

ADAC Laboratories Recalls

All product recalls associated with ADAC Laboratories.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Mar 2004

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

ADAC Laboratories: Philips Pinnacle3 Version 6.4a Radiation Therapy Planning...

Dose delivery in the wrong location may occur when using a Elekta Leksell headframe.

FDAMar 3, 2004Nationwide• ADAC Laboratories

ADAC Laboratories: Pinnacle3 Radiation Therapy Planning System, Version 7.0e...

A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe.

FDAMar 3, 2004Nationwide• ADAC Laboratories

ADAC Laboratories: Philips ADAC Pinnacle3 Version 6.4a Radiation Therapy Pla...

Dose delivery in the wrong location may occur when using a Elekta Leksell headframe.

FDA

Mar 3, 2004

Nationwide

• ADAC Laboratories