Recalls / —
—#106244
Product
Terumo CDI 101 Hematocrit/Oxygen Saturation Monitoring System. Monitors blood/oxygen saturation, hematocrit and hemoglobin levels.
- FDA product code
- DRY — Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
- Device class
- Class 2
- Medical specialty
- Cardiovascular
- Affected lot / code info
- Catalog number: 101 and Serial Numbers: 0503, 1000, 1017, 1070, 1071, 1073, 1074, 1076, 1077, 1080, 1082, 1083, 1107-1110, 1115-1117,1124,1126-1134, 1136, 1137, 1139-1146, 1148-1152, 1154-1156, 1159-1162, 1164-1166, 1168-1177, 1182, 1185-1190, 1192,1193, 1195, 1197, 1198, 1225, 1228, 1229, 1237, 1239-1241,1243-1245,1247, 1249-1326, 1332-1339, 1344-1347, 1349, 1350-1363, 1365-1409, 1411-1436,1438, 1440-1447, 1449-1453, 1455-1463,1465-1482,1484-1492,1494-1552,1555-1565, 1567-1600,1602,1605-1607,1609-1611,1613-1623,1625-1629,1632-1651,1653, 1655-1660, 1662-1664, 1666, 1667,1669-1679,1681-1684,1686,1689-1691, 1693-1710,1712-1715,1717-1750,1752-1757,1759-1771,1773-1785,1787,1788,1790-1809, 1811-1831,1833,1838,1839,1855-1858,1866, and TK001-TK011.
Why it was recalled
Inaccurate readings. Software contains unused (turned off) accuracy correction factors for slope (gain) and offset (bias) for Hematocrit/Saturation calculations. The accuracy on any cuvette size did not meet the specifications.
Root cause (FDA determination)
Software design
Action the firm took
Terumo sent an "URGENT MEDICAL DEVICE CORRECTION" letter dated November 1, 2010 to all affected customers. The letter identified the product, problem, and the actions to be taken by the customers. Contact Terumo CVS Customer Service at 1-800-521-2818 for questions or concerns.
Recalling firm
- Firm
- Terumo Cardiovascular Systems Corporation
- Address
- 6200 Jackson Road, Ann Arbor, Michigan 48103-9586
Distribution
- Distribution pattern
- Worldwide Distribution.
Timeline
- Recall initiated
- 2010-11-01
- Posted by FDA
- 2013-02-12
- Terminated
- 2013-11-08
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #106244. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.