🔍 RecallPedia

Aspiration Syringe Kit, REF: MVSK60

Class I - Dangerous
🏥 Medical Devices Recalled: October 20, 2021 MICROVENTION Surgical Instruments Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461
  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:
MICROVENTION INC.
Reason for Recall:
Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Aspiration Syringe Kit, REF: MVSK60

Product Codes/Lot Numbers:

Lot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0202-2022

Related Recalls

Flow Re-Direction Endoluminal Devices: FRED 27, REF: FRED5019, FRED5029, FRED4528, FRED4026, FRED5526, FRED4508, FRED5514, FRED3536, FRED3511, FRED5014, FRED3516, MV-F451827; FRED X 27, REF: XFRED4017-MVE, XFRED4528-MVE, MV-F501427X, XFRED4518-MVE, XFRED5526-MVE, XFRED4539-MVE, FREDX5522-PMA, FREDX3522-PMA, FREDX4525-PMA, FREDX5015-PMA, FREDX5532-PMA, FREDX4013-PMA, FREDX3513-PMA, FREDX4515-PMA, FREDX3517-PMA, MV-F352427X

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Class I - Dangerous

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