# FDA recall Z-2738-2024

> **Agfa N.V.** · Class II · device recall initiated 2024-07-29.

## Product

DR 800. Digital Radiography X-ray System.

## Reason for recall

Potential for the front lever chain of the DR 800 table to fail.

## Distribution

Worldwide - US Nationwide distribution in the states of CA, FL, IL, IN, KS, LA, MA, MO, NJ, NC, OH, OK, SC, VA, WV, WI; and the countries of AU, BE, BW, CA, CO, CZ, DE, ES, FR, GB, GR, IL, IN, IT, KZ, MX, PL, RS, UZ, ZA.

## Key facts

- **Recall number:** Z-2738-2024
- **Recalling firm:** Agfa N.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-29
- **Report date:** 2024-09-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mortsel, Belgium

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2738-2024

## Citation

> AI Analytics. FDA recall Z-2738-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2738-2024. Source: US FDA. Licensed CC0.

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