🔍 RecallPedia

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S

Class I - Dangerous
🏥 Medical Devices Recalled: October 27, 2020 Mani, Inc. - Kiyohara Facility Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Codes: V180077300, Exp Date: 2020/10 and V200009500, EXp Date: 2022/03
  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:
Mani, Inc. - Kiyohara Facility
Reason for Recall:
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MANI TROCAR KIT 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials during ophthalmic surgery, Ref: MTK 23S

Product Codes/Lot Numbers:

Lot Codes: V180077300, Exp Date: 2020/10 and V200009500, EXp Date: 2022/03

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0557-2021

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