PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands Veradius Unity, Model #718132 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Veradius Unity, Model #718132
Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
Lot Codes / Batch Numbers
Wireless Foot switch 3P : 459801238191 Wireless Foot switch 3P: 459801238231
Products Sold
Wireless Foot switch 3P : 459801238191 Wireless Foot switch 3P: 459801238231
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands is recalling Veradius Unity, Model #718132 due to Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.
Recommended Action
Per FDA guidance
On December 2, 2021, the firm issued Urgent Medical Device Correction letters to affected customers. The Medical Device Correction includes the following instructions for the Customer: o Ensure that the wired foot switch is always connected to the system. o Immediately start using the wired foot switch or hand switch in the event the wireless foot switch loses connection. o Perform a daily check for damage and correct functioning of the hand switch and wired foot switch as described by the User Routine Checks section in your Instruction for Use. o Circulate this notice to all users of this device so that they are aware of the issue./ o Place this Medical Device Correction with the documentation of the Philips Zenition 50, Zenition 70 or Veradius Unity system. o Return the attached reply form to Philips to confirm that: 1. The Zenition 50, Zenition 70 and Veradius Unity systems wired foot switch is connected to the system 2. The users of the system have reviewed and understood this Medical Device Correction. If you need further information or support concerning this issue, please contact your local Philips representative: 1-800-722-9377.
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 noticeDistribution
As reported by FDA
AZ, CA, FL, GA, HI, IL, KS, KY, ME, MD, MA, MI, MN, MS, NE, NV, NJ, NY, NC, OH, PA, TN, TX, VA, WA, WV
Page updated: Jan 10, 2026