Eclipse Infusion Pump, 250 ml X 250 ml per hour) Part 5001247
FDA Recall Z-0312-04 · Posted 2004-01-09
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Recalling FirmI-Flow Corporation
Recall StatusTerminated
Product CodeMEB
Date Initiated2002-08-19
Date Terminated2005-01-04
Product Quantity144
Reason for Recall
Slower than expected infusion of medications, such as antibiotics.
Firm Action
All customers were contacted by telephone on 8/19/2002. Letters were also sent dated 8/27/2002. Recall is complete.
Root Cause
Other
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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