Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot Number 73H1600207
  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:
Teleflex Medical
Reason for Recall:
Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.

Product Codes/Lot Numbers:

Lot Number 73H1600207

Distribution:

Distributed in: KS

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1193-2018

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