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U.S. Department of Health and Human Services

Class 2 Device Recall Allura Xper FD20/10

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 Class 2 Device Recall Allura Xper FD20/10see related information
Date Initiated by FirmSeptember 24, 2007
Date PostedDecember 07, 2007
Recall Status1 Terminated 3 on May 03, 2012
Recall NumberZ-0330-2008
Recall Event ID 44959
510(K)NumberK033737 
Product Classification Angiographic x-ray system - Product Code IZI
ProductAllura Xper FD20/10, Release 1.2, Philips Medical Systems, Bothell, WA 98021
Code Information Serial numbers affected:  18, 19, 22, 23, 24, 32, 33, 34, 36, 38, 52, 54, 56, 67, 68, 69, 71, 73, 74, 82, 84, 94, 99, 100, 102, 103, 106, 108, 112, 113, 116, 124, 125, 126, 131, 133, 141, 142, 148, 154, 157, 173, 174, 176, 178, 187, 191, 192, 197, 199, 212, and 691.
FEI Number 1000524572
Recalling Firm/
Manufacturer		 Philips Medical Systems North America Co. Phillips
22100 Bothell Everett Hwy
Bothell WA 98021-8431
For Additional Information ContactSarah Baxter
425-487-7602
Manufacturer Reason
for Recall		Inaccurate anatomical measurements when using the optional SmartMask feature
FDA Determined
Cause 2		Device Design
ActionThe recalling firm sent customers an Urgent Device Correction notification letter dated 09/21/07 via certified mail - return receipt requested. This notification provided a short term work around for the device defect. For a permanent fix, the recalling firm is developing software update to check for mismatch at the start of a subtracted fluoroscopy run, and will contact customers to schedule an install. Installation is expected to begin 10/2007 and be completed 06/2008.
Quantity in Commerce53 units
DistributionNationwide
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = IZI
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