IceRod" 1.5 MRI 90¿ Cryoablation Needle¿

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    UPN: FPRPR3195 UDIs: 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297 Batch Numbers: U1406, U1407, U1370, U1369, U1041, U1042, U0611, U0610, U0501, U0419, U0447, U0444, U0418, U0322, U0323, U0211, U0243, U0244, U0208, U0209, U0210, U0189, U0188, U0175, U0174, U0031, U0164, U0005, U0004, U0002, U0001, T0786, T0785, T0664, T0665, T0649, T0650, T0562, T0561, T0452, T0451, T0445, T0441, T0440, T0364, T0365, T0361, T0360, T0192, T0193, T0179, T0180, A7213, A6715, A6714, A6712, A6711, A6672, A6673, A2093, A2094, A2036, A2037, A2023, A2024, A2011, A2012, A1986, A1987, A1949, A1948, A1944, A1943, A1925, A1924, A1884, A1883, A1839, A1837, A1838, A1832, A1833, A1758, A1759, A1756, A1757, A1648, A1647, A1572, A1573, A1555, A1556, A1534, A1334, A1321, A1322, A1318, A1319, A1200, A1198, A1201, A1199, A1070, A1071, A1068, A1067, A1002, A1001, A0882, A0883, A0878, A0879, A0737, A0738
  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:
Boston Scientific Corporation
Reason for Recall:
Complaint trend regarding needle shaft gas leaks.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

IceRod" 1.5 MRI 90¿ Cryoablation Needle¿

Product Codes/Lot Numbers:

UPN: FPRPR3195 UDIs: 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297 Batch Numbers: U1406, U1407, U1370, U1369, U1041, U1042, U0611, U0610, U0501, U0419, U0447, U0444, U0418, U0322, U0323, U0211, U0243, U0244, U0208, U0209, U0210, U0189, U0188, U0175, U0174, U0031, U0164, U0005, U0004, U0002, U0001, T0786, T0785, T0664, T0665, T0649, T0650, T0562, T0561, T0452, T0451, T0445, T0441, T0440, T0364, T0365, T0361, T0360, T0192, T0193, T0179, T0180, A7213, A6715, A6714, A6712, A6711, A6672, A6673, A2093, A2094, A2036, A2037, A2023, A2024, A2011, A2012, A1986, A1987, A1949, A1948, A1944, A1943, A1925, A1924, A1884, A1883, A1839, A1837, A1838, A1832, A1833, A1758, A1759, A1756, A1757, A1648, A1647, A1572, A1573, A1555, A1556, A1534, A1334, A1321, A1322, A1318, A1319, A1200, A1198, A1201, A1199, A1070, A1071, A1068, A1067, A1002, A1001, A0882, A0883, A0878, A0879, A0737, A0738

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0678-2021

Related Recalls

Class I - Dangerous

Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

Aug 20, 2025 Implants & Prosthetics View Details →
Class I - Dangerous

Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

Aug 20, 2025 Implants & Prosthetics View Details →
Class I - Dangerous

Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

Aug 20, 2025 Other Medical Devices View Details →