# FDA recall Z-1156-2024

> **PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.** · Class II · device recall initiated 2024-01-02.

## Product

Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used with affected systems.    Allura Xper Model Name - Model Number:    Allura Xper FD10  722003  722010  722026;    Allura Xper FD10/10  722005  722011  722027;  Allura Xper FD10C  722001;  Allura Xper FD20  722006  722012  722028;  Allura Xper FD20 Biplane  722008  722013;  Allura Xper FD20 Biplane OR Table  722025;  Allura Xper FD20 OR Table  722023  722035;  Allura Xper FD20/10  722029;  Allura Xper FD20/15  722058;    Allura Xper FD20/20  722038;  Allura Xper FD20/20 OR Table  722039;    (Allura Centron - 722400 is impacted by this recall, but Allura Centron systems are not distributed in the United States.)

## Reason for recall

Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.

## Distribution

Worldwide Distribution: US nationwide including states of: AL, AK, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, WV, & WY; and OUS (International) to countries of: Afghanistan, Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Fiji, Finland, France, French Polynesia, Gabon, Georgia, Germany, Ghana, Greece, Guadeloupe, Guinea, Honduras, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Macedonia, 

## Key facts

- **Recall number:** Z-1156-2024
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-02
- **Report date:** 2024-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Best, N/A, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1156-2024

## Citation

> AI Analytics. FDA recall Z-1156-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1156-2024. Source: US FDA. Licensed CC0.

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