DEMO No Needle Corrugated Carton 20 U/D recall
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2568-03
Why was DEMO No Needle Corrugated Carton 20 U/D recalled?
There is a potential for "No Needle Demo Units" to contain a needle.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: (01)10385609021039(17)XXXXXX(10)XXXXXXXX Lot Number: DM218024
- Product
- DEMO No Needle Corrugated Carton 20 U/D, Part Number 2568-03
- Recalling firm
- Valeritas, Incorporated
- Quantity
- 852 devices
- Distribution
- Nationwide within U.S.
- Recall date
- November 6, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)