Venoscope LLC Venoscope Neonatal Transilluminator, Model NT01 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Venoscope Neonatal Transilluminator, Model NT01
Brand
Venoscope LLC
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
The product is not lot coded on the exterior of the device and could not be identified by the consignee without disassembling the device to find the lack of an identifying mark.
Venoscope LLC is recalling Venoscope Neonatal Transilluminator, Model NT01 due to Excessive heating due to incorrect wire assembly process.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Excessive heating due to incorrect wire assembly process.
Recommended Action
Per FDA guidance
The firm notified its consignees about the problem beginning on 04/28/2006 and requested the consignee (nurses and distributors) open the battery compartment and check for the absence of an identifying mark (there are no exterior lot numbers). The recalling firm requested the return of all lights which had no identifying marks inside the battery compartment.
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