# FDA recall Z-0952-2024

> **Philips North America** · Class II · device recall initiated 2024-01-03.

## Product

Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.

## Reason for recall

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-0952-2024
- **Recalling firm:** Philips North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-03
- **Report date:** 2024-02-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0952-2024

## Citation

> AI Analytics. FDA recall Z-0952-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0952-2024. Source: US FDA. Licensed CC0.

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