PKG, 3MM PEEK MONOPOLAR HANDLE, P/N 0250282045 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    843744 847017 942768 943108 943436 943515 944197 944825 945711 1040927 1042098 1042468 1042513 1042514 1042957 1043819 1045057 1045626 1046584 1140930 1141656 1142239 1144237 1144342 1145343 1146674 1147037 1242641 1243948 1246163H 1340920H 1341894 1341894H 1344199 1344872 1344990 1345272 1345272H 1346215 1346215H 1346684 1440429 1441830
  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:
Stryker Endoscopy
Reason for Recall:
The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

PKG, 3MM PEEK MONOPOLAR HANDLE, P/N 0250282045 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.

Product Codes/Lot Numbers:

843744 847017 942768 943108 943436 943515 944197 944825 945711 1040927 1042098 1042468 1042513 1042514 1042957 1043819 1045057 1045626 1046584 1140930 1141656 1142239 1144237 1144342 1145343 1146674 1147037 1242641 1243948 1246163H 1340920H 1341894 1341894H 1344199 1344872 1344990 1345272 1345272H 1346215 1346215H 1346684 1440429 1441830

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0773-2015

Related Recalls

When operating the device in high flow mode (40L/min, 15 mmHg) and connecting to a house gas inlet source, within seconds of insufflating the flow rate would drop to 0L/min and the red Check Gas Supply symbol would appear on the display, immediately suspending insufflation.

Mar 28, 2016 Diagnostic Equipment Nationwide View Details →

Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy Probes due to reports of fragments of the probe breaking off into the patient.

Jun 3, 2015 Implants & Prosthetics Nationwide View Details →

The parameters provided in the Laparoscopic Manual Instruments Instructions for Use (IFU 1000-401-070 Revision G or prior) do not support the unwrapped Gravity cycle and the Ethylene Oxide cycle sterilization methods

Nov 17, 2014 Surgical Instruments Nationwide View Details →