510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1822-2017Class II

The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper...

Philips North America LLC / initiated 2017-03-22 / Terminated / root cause: packaging

Philips Electronics North America Corporation began a recall of The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 722003... on . FDA classified it as Class II and gives the reason as "Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room...". As of , the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number
Z-1822-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Philips North America LLC
Product
The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 722003; Allura Xper FD10/10 722005; Allura Xper FD20 722006; Allura Xper FD20/10 and FD20/20 722008; Allura Xper FD10 722010; Allura Xper FD10/10 722011; Allura Xper FD20 722012; Allura Xper FD20 biplane 722013; Allura Xper FD10 OR Table 722014; Allura Xper FD20 OR Table 722015; Allura Xper FD10/10 OR Table 722019; Allura Xper FD20 Biplane OR Table 722020; Allura Xper FD10 OR Table 722022; Allura Xper FD20 OR Table 722023; Allura Xper FD10/10 OR Table 722024; Allura Xper FD20 Biplane OR Table 722025; Allura CV20 722031
Product code
OWB Interventional Fluoroscopic X-Ray System
Reason for recall
Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.
Root cause tag
packaging
FDA root cause
Under Investigation by firm
Action
Consignees were notified of the recall via letter sent on 3/22/2017. The letter explains the issue, actions that should be taken by the customer, and actions to be taken by Philips.
Quantity in commerce
6992 (total distributed for all products)
Distribution
Nationwide, worldwide including Canada
Product codes and lots
Devices with a Laird Chiller.

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1822-2017
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1820-2017Class IITerminatedVoluntary: Firm initiated
Z-1821-2017Class IITerminatedVoluntary: Firm initiated
Z-1822-2017Class IITerminatedVoluntary: Firm initiated