The Recall Desk
ModerateFDA (Devices)·Z-1065-2026·Announced 2026-01-21

Allura Xper FD10/10, model 722005, recalled over a missing drip tray

Philips Medical Systems Nederland is recalling 14 units of the Allura Xper FD10/10, model 722005, because the drip tray beneath the cooling unit may not have been installed.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: Scored 2 because the record's stated consequence is a system shutdown, with no patient harm or reported injury.

Plain-English summary

The Philips Allura Xper FD10/10, model number 722005, is being recalled by Philips Medical Systems Nederland B.V.

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. The firm states this could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

The record lists 14 units under model number 722005, with no UDI-DI given, and affected serial numbers listed in the enforcement record. Distribution was worldwide, including nationwide in the United States and to a wide range of other countries. The FDA has classified the action as Class II.

The stated consequence in the enforcement record is system shutdown, and no injuries are reported. Facilities should follow Philips' instructions.

The recalled product

Product
Allura Xper FD10/10; Model Number: 722005;
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Category
Medical Device — Interventional X-ray
Hazard
Affected units
14

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (17)

  • Model Number: 722005
  • System Product Name: Allura Xper FD10/10
  • UDI-DI: N/A
  • Serial Numbers: 93
  • 269
  • 530
  • 306
  • 307
  • 247
  • 53
  • 401
  • 141
  • 531
  • 184
  • 75
  • 276
  • 36

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 16 recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 16 products in this recall →

Related recalls

Same manufacturer · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

See all →

Same hazard · missing component

See all →