3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030NS, general surgery drape

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UDI/DI (01)50707387029352, Lot numbers: 33JPRN, 33JPWY, 33JR98, 33KLEY, 33KLME
  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:
3M Healthcare Business
Reason for Recall:
During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Additionally, 3M has observed an increase in reported adhesive related skin injuries for these affected lots.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

3M Steri-Drape, Medium Drape with Adhesive Aperture, REF 1030NS, general surgery drape

Product Codes/Lot Numbers:

UDI/DI (01)50707387029352, Lot numbers: 33JPRN, 33JPWY, 33JR98, 33KLEY, 33KLME

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0258-2023

Related Recalls

During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Additionally, 3M has observed an increase in reported adhesive related skin injuries for these affected lots.

Oct 6, 2022 Other Medical Devices View Details →