# FDA recall Z-1744-2022

> **Philips Medical Systems (Cleveland) Inc** · Class II · device recall initiated 2022-08-30.

## Product

Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.

## Reason for recall

When computing a radiation dose in the system, the exported dose information is incorrect when there is more than one beam attached to the prescription and certain options are selected on the Edit Prescription screen.

## Distribution

Distribution was made to CA, FL, GA, IA, IL, MA, MD, ME, MI, MN, NJ, NM, NV, NY, OH, OK, RI, SC, TN, TX, and WA.  There was government distribution and no military distribution.  Foreign distribution was made to Australia, Austria, Belgium, China, France, Germany, Italy, Japan, Jordan, Lebanon, Poland, Portugal, Romania, Russian Federation, Singapore, Spain, Switzerland, Taiwan, Thailand, and United Kingdom.

## Key facts

- **Recall number:** Z-1744-2022
- **Recalling firm:** Philips Medical Systems (Cleveland) Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-08-30
- **Report date:** 2022-09-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gainesville, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1744-2022

## Citation

> AI Analytics. FDA recall Z-1744-2022. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1744-2022. Source: US FDA. Licensed CC0.

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