Philips Medical Systems North America Co. Phillips Allura FD 10 FC, X-Ray System, angiographic - a monoplane, digital Allura FD (flat detector) with a 10' Image Intensifier (II). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Allura FD 10 FC, X-Ray System, angiographic - a monoplane, digital Allura FD (flat detector) with a 10' Image Intensifier (II).
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
site numbers provided in the product listing for Z-0366-2007
Products Sold
site numbers provided in the product listing for Z-0366-2007
Philips Medical Systems North America Co. Phillips is recalling Allura FD 10 FC, X-Ray System, angiographic - a monoplane, digital Allura FD (flat detector) with a due to Movement of the AD5 table or Lateral C-arm (LARC). The table and/or LARC will not move upon request, will move slowly when movement is requested or . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Movement of the AD5 table or Lateral C-arm (LARC). The table and/or LARC will not move upon request, will move slowly when movement is requested or will not stop moving when requested.
Recommended Action
Per FDA guidance
On 12/14/05 and 12/20/06 the firm issued a letter dated 12/12/06 to their customers. The letter explains the problem and states that the firm will be performing mandatory upgrades to correct the situation. Consignees will be contacted to arrange for service.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026