Flexible Intubation Fiberscope, Model # 11301AB1

Class I - Dangerous

What Should You Do?

Check if you have this product:
Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769
Do not eat it: Even if it looks and smells fine, do not consume this product.
Throw it away or return it: You can return the product to the store for a full refund.
Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
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.

Company:: Karl Storz Endoscopy
Reason for Recall:: The action is being initiated due to intubation scopes improperly manufactured with a double port luer instead of a single port luer.
Classification:: Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
Status:: terminated

Flexible Intubation Fiberscope, Model # 11301AB1

Lot numbers: 2183827, 2195794, 2215741, 2229258, 2235373, 2248169, 2193769

Distributed in: US, VA, MO, CA, OH, NM, NY, CO, LA, ME

Always verify recall information with the official FDA source:

FDA Recall Number: Z-2447-2019

Karl Storz Endoscopy

Class I - Dangerous

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Dec 19, 2024 Other Medical Devices Nationwide View Details →

Karl Storz Endoscopy

Class I - Dangerous

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Dec 19, 2024 Other Medical Devices Nationwide View Details →

Karl Storz Endoscopy

Class I - Dangerous

Scope IFUs contain a reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

Dec 19, 2024 Other Medical Devices Nationwide View Details →