Philips Medical Systems Sales & Service Region No. America Diagnost 94 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Diagnost 94
Brand
Philips Medical Systems Sales & Service Region No. America
Lot Codes / Batch Numbers
See Diagnost 96 above
Products Sold
See Diagnost 96 above
Philips Medical Systems Sales & Service Region No. America is recalling Diagnost 94 due to Potential for table to move by itself. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for table to move by itself
Recommended Action
Per FDA guidance
The firm issued a letter dated 8/10/03 informing the consignees of the error and advising that a service employee will be visiting each site for software upgrade.
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