Philips Medical Systems North America Co. Phillips Diagnost 76 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Diagnost 76
Brand
Philips Medical Systems North America Co. Phillips
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Site Number: 82943 - this was accidently identified as a Dignost 76 and is actually an EasyDiagnost Digital system
Philips Medical Systems North America Co. Phillips is recalling Diagnost 76 due to The x-ray system fail to meet the requirements of 21 CFR 1020.32(d)(2)(ii) when a specific tube failure occurs involving fluoroscopy of large patients. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The x-ray system fail to meet the requirements of 21 CFR 1020.32(d)(2)(ii) when a specific tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch
Recommended Action
Per FDA guidance
A Customer Notification letter describing the potential grid switch failure and actions planned by Philips to correct the problem will be sent to all users of the affected systems during the week of July 6, 2009.
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