Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BTNL

Class I - Dangerous
🏥 Medical Devices Recalled: February 28, 2024 Covidien Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Product Number/CFN: OMS-T12BTNL; UDI/DI: 20884521552446, 10884521552449; Lot Serial Number: P0L1444, P0L1444, P0M1932, P0M1932, P1A1491, P1A1491, P1B0649, P1B0649, P1B1560, P1B1560, P1D0399, P1D0399, P1G0142, P1G0142, P1G1132, P1G1132, P1G1365, P1J1046, P1J1179, P1J1179, P1J1213, P1J1213, P1L0002, P1M0637, P1M0637, P1M0838, P1M0838, P2A0608, P2A0608, P2B0747, P2B0747, P2B0981, P2B0982, P2B0982, P2C0229, P2C0229, P2C0690, P2C0710, P2C0710, P2F0161, P2G0536, P2G0536, P2G0537, P2G0537, P2H0423, P2J0274, P2J0274, P2J0283, P2J0283, P2K0193, P2K0193, P2K0567, P2M0165, P2M0165, P2M0276, P2M0276, P3A0094, P3B0040, P3B0041, P3B0520, P3B0520, P3D0250, P3D0250, P3E0457, P3F0078, P3F0573, P3G0330, P3G0330, P3H1178, P3H1261, P3J1164;
  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:
Covidien, LP
Reason for Recall:
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BTNL

Product Codes/Lot Numbers:

Product Number/CFN: OMS-T12BTNL; UDI/DI: 20884521552446, 10884521552449; Lot Serial Number: P0L1444, P0L1444, P0M1932, P0M1932, P1A1491, P1A1491, P1B0649, P1B0649, P1B1560, P1B1560, P1D0399, P1D0399, P1G0142, P1G0142, P1G1132, P1G1132, P1G1365, P1J1046, P1J1179, P1J1179, P1J1213, P1J1213, P1L0002, P1M0637, P1M0637, P1M0838, P1M0838, P2A0608, P2A0608, P2B0747, P2B0747, P2B0981, P2B0982, P2B0982, P2C0229, P2C0229, P2C0690, P2C0710, P2C0710, P2F0161, P2G0536, P2G0536, P2G0537, P2G0537, P2H0423, P2J0274, P2J0274, P2J0283, P2J0283, P2K0193, P2K0193, P2K0567, P2M0165, P2M0165, P2M0276, P2M0276, P3A0094, P3B0040, P3B0041, P3B0520, P3B0520, P3D0250, P3D0250, P3E0457, P3F0078, P3F0573, P3G0330, P3G0330, P3H1178, P3H1261, P3J1164;

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1471-2024

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