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Terminated

Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets.

FDA Recall Z-0819-2007 · Posted 2007-05-31

Recalling FirmB. Braun Medical, Inc.
Recall StatusTerminated
Product CodeFPA
Date Initiated2007-04-18
Date Terminated2008-04-22
Product Quantity2.5 million for all products

Reason for Recall

Secondary infusion backs up into primary container.

Firm Action

The recalling firm issued Product Removal Notices on 4/20/07 via certified priority mail. The notice informed the customer of the problem and the need to return the product.

Root Cause

Other

Distribution Pattern

Nationwide and Canada.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K955585V2 INJECTION SITEB.Braun Medical, Inc. · 1996-05-15K904518VOLUMETRIC INFUSION PUMPKendall Mcgaw Laboratories, Inc. · 1990-10-17

Official Source

View FDA Recall →

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

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