FDA Device Recalls

Recalls / —

—#184548

Product

IceRod" i-Thaw" Prostate Cryoablation Kit

FDA product code
GEH — Unit, Cryosurgical, Accessories
Device class
Class 2
Medical specialty
General, Plastic Surgery
510(k) numbers
K060390
Affected lot / code info
UPN: FPRPR3572  UDIs: 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983  Batch Numbers: U1423, U1422, U1329, U1227, U1091, U1128, U1127, U1090, U0976, U1011, U0919, U0917, U0868, U0869, U0738, U0739, U0403, U0404, U0297, U0296, U0256, U0255, U0217, U0218, U0034, U0176, U0033, U0032, U0016, U0040, U0015, T0759, T0758, T0731, T0651, T0634, T0524, T0507, T0502, T0470, T0429, T0401, T0391, T0372, T0351, T0319, T0306, T0281, T0271, T0247, T0198, T0189, T0161, T0084, T0074, T0008, A7231, A7212, A7206, A7188, A7040, A7018, A6983, A6898, A6886, A6878, A6867, A6864, A6843, A6824, A6787, A6718, A6687, A6671, A6663, A6646, A2138, A2124, A2100, A2099, A2082, A2053, A2013, A2001, A1994, A1975, A1945, A1892, A1761, A1748, A1688, A1685, A1612, A1596, A1519, A1502, A1497, A1479, A1447, A1424, A1405, A1378, A1377, A1356, A1347, A1340, A1320, A1227, A1218, A1202, A1187

Why it was recalled

Complaint trend regarding needle shaft gas leaks.

Root cause (FDA determination)

Under Investigation by firm

Action the firm took

Customers will be sent a product advisory via overnight mail.

Recalling firm

Firm
Boston Scientific Corporation
Address
1 Scimed Pl, Maple Grove, Minnesota 55311-1565

Distribution

Distribution pattern
Nationwide

Timeline

Recall initiated
2020-11-18
Status
—

Source: openFDA Device Recall endpoint. Recall record ID #184548. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.