🔍 RecallPedia

DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03

Class I - Dangerous
🏥 Medical Devices Recalled: July 3, 2019 Valeritas, Incorporated Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI: (01)10385609020039(17)XXXXXX(10)XXXXXXXX Lot Numbers: DM218001 DM218002 DM218003 DM218004 DM218005 DM218006 DM218020 DM218025 DM218034 DM218035 DM218036
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Valeritas, Incorporated
Reason for Recall:
There is a potential for "No Needle Demo Units" to contain a needle.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03

Product Codes/Lot Numbers:

UDI: (01)10385609020039(17)XXXXXX(10)XXXXXXXX Lot Numbers: DM218001 DM218002 DM218003 DM218004 DM218005 DM218006 DM218020 DM218025 DM218034 DM218035 DM218036

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0195-2020

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