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Terminated

Easypump L T 60-24 infusion pump

FDA Recall Z-0585-06 · Posted 2006-03-07

Recalling FirmI-Flow Corporation
Recall StatusTerminated
Product CodeMEB
Date Initiated2006-01-17
Date Terminated2007-02-05
Product Quantity549

Reason for Recall

The sterile pack may contain the wrong infusion pump inside.

Firm Action

The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.

Root Cause

Other

Distribution Pattern

France only

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K052117I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOCK, HOMEPUMP, EASYPUMP)I-Flow Corp. · 2005-09-09K932740HOMEPUMP NSFBlock Medical, Inc. · 1993-10-06

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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