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Recall Observatory FDA recall evidence

Device product

20-Pole Eco Cable, Catalog #EM-5050-060 Product Usage: The 20-Pole Eco Cable is intended to be used as an interface cable between the LASSO NAV Eco Catheter and CARTO 3 System.

Z-1023-2013

March 05, 2013

Class II

Product summary

Firm
Biosense Webster, Inc.
Event
Event 64579
Status
Terminated
Classification
Class II
Quantity
54 units
Official record key
device-enforcement:Z-1023-2013

Official wording

Reason: Biosense is recalling the 20-Pole Eco Cable because it was incorrectly calibrated. When a catheter is connected to an affected to an affected 20-Pole Eco Cable, the catheter will not be recognized by the impacted 54 cable serial numbers within the field.

Code information: Impacted serial Numbers: 120, 132, 134,136, 151, 342, 350, 354, 356, 363, 368, 373, 379, 380, 384, 385, 402, 405, 424, 919, 953, 954, 960, 963, 968, 970, 977, 980, 993, 998, 1001, 1123, 1148, 1378, 1596, 1729, 1745, 1747, 1749, 1750, 1751, 1753, 1754, 1758, 1759, 1760, 1761, 1797, 1799, 1802, 1803, 1804, 1805. Lot Numbers: P1210, P1220, P1221, P1231.

Distribution pattern: Worldwide Distribution - USA (Nationwide) including the states of: DE, NL, CH, FR, GB, DK.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Biosense is recalling the 20-Pole Eco Cable because it was incorrectly calibrated. When a catheter is connected to an affected to an affected 20-Pole Eco Cable, the catheter will not be recognized by the impacted 54 cable serial numbers within the field.

Field note

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