Valeritas, Incorporated DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
Brand
Valeritas, Incorporated
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
UDI: (01)10385609020039(17)XXXXXX(10)XXXXXXXX Lot Numbers: DM218001 DM218002 DM218003 DM218004 DM218005 DM218006 DM218020 DM218025 DM218034 DM218035 DM218036
Valeritas, Incorporated is recalling DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03 due to There is a potential for "No Needle Demo Units" to contain a needle.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for "No Needle Demo Units" to contain a needle.
Recommended Action
Per FDA guidance
On July 3, 2019, Valeritas issued notices to customers via first class U.S. postal service. The removal strategy is to notify active HCP office accounts from the manufacturing start date of effected product (January 2018) who may have No Needle Demo units in their possession. The removal letter instructs HCP offices to dispose of any No Needle Demo product on hand and acknowledgement by signing and returning the removal letter as instructed.
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