Part #: SAM XT-M, Model: Tactical Black or Military

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot #: XT1711, XT1712, XT1713, XT1715, XT1719, XT1720, XT1721, XT1722, XT1723, XT1724, XT1725, XT1726, XT1727, XT1728, XT1729, XT1730, XT1731, XT1732, XT1734, XT1737, XT1738, XT1740, XT1742, XT1743, XT1744, XT1745, XT1746, XT1747, XT1748, XT1749, XT1750, XT1751, XT1752, XT1801, XT1803, XT1804, XT1805, XT1806, XT1807, XT1808, XT1809, XT1810, XT1811
  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:
The Seaberg Company Inc
Reason for Recall:
Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Part #: SAM XT-M, Model: Tactical Black or Military

Product Codes/Lot Numbers:

Lot #: XT1711, XT1712, XT1713, XT1715, XT1719, XT1720, XT1721, XT1722, XT1723, XT1724, XT1725, XT1726, XT1727, XT1728, XT1729, XT1730, XT1731, XT1732, XT1734, XT1737, XT1738, XT1740, XT1742, XT1743, XT1744, XT1745, XT1746, XT1747, XT1748, XT1749, XT1750, XT1751, XT1752, XT1801, XT1803, XT1804, XT1805, XT1806, XT1807, XT1808, XT1809, XT1810, XT1811

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2226-2018

Related Recalls

Class I - Dangerous

Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.

May 2, 2018 Other Medical Devices Nationwide View Details →
Class I - Dangerous

Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.

May 2, 2018 Infusion Pumps Nationwide View Details →