BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of contrast media up to a rate of 8 ml/sec and at a maximum of 325 psi fluid pressure.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    LOT: 257828, 258294, 259262, 260814, 260173, 261861, 264561, 266804, 266805, 267191, 269121
  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:
Access Scientific LLC
Reason for Recall:
Saline Flush Syringe compromised sterility due to holes in the packaging.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of contrast media up to a rate of 8 ml/sec and at a maximum of 325 psi fluid pressure.

Product Codes/Lot Numbers:

LOT: 257828, 258294, 259262, 260814, 260173, 261861, 264561, 266804, 266805, 267191, 269121

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1972-2020

Related Recalls

Convenience kit mislabeled with the incorrect catheter effective length on the device label and the packaging label. Use may lead to a delay or interruption of treatment and user dissatisfaction or annoyance.

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Saline Flush Syringe compromised sterility due to holes in the packaging.

Apr 23, 2020 Surgical Instruments Nationwide View Details →

Saline Flush Syringe compromised sterility due to holes in the packaging.

Apr 23, 2020 Surgical Instruments Nationwide View Details →