🔍 RecallPedia

LYSO Disk(TM) labeled as containing Actinomyces odontolyticus. Each LYSO Disk" unit contains six lyophilized pellets of a single microorganism strain, in a glass vial. Each vial is sealed and contains a desiccant to prevent adverse moisture accumulation. A LYFO Disk" catalog number ends in L.

Class I - Dangerous
🏥 Medical Devices Recalled: March 2, 2017 Microbiologics Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Catalog Number: 0939L, Lot Number: 939-47-1, UDI: 10845357022728
  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:
Microbiologics Inc
Reason for Recall:
Potential for product labeled as Actinomyces odontolyticus is actually Eggerthella lenta.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

LYSO Disk(TM) labeled as containing Actinomyces odontolyticus. Each LYSO Disk" unit contains six lyophilized pellets of a single microorganism strain, in a glass vial. Each vial is sealed and contains a desiccant to prevent adverse moisture accumulation. A LYFO Disk" catalog number ends in L.

Product Codes/Lot Numbers:

Catalog Number: 0939L, Lot Number: 939-47-1, UDI: 10845357022728

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0637-2022

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