Z-0819-2007

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

Name: Z-0819-2007 Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets
Creator: B. Braun Medical, Inc.
Published: 2007-04-18
License: https://open.fda.gov/license/

B Braun Medical Inc / initiated 2007-04-18 / Terminated

FDA source

B. Braun Medical, Inc. began a recall of Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets on 2007-04-18. The reason FDA records is "Secondary infusion backs up into primary container". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0819-2007
Status: Terminated
Initiated: 2007-04-18
Posted: 2007-05-31
Terminated: 2008-04-22
Recalling firm: B Braun Medical Inc
Product: Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets.
Product code: FPA Set, Administration, Intravascular
Reason for recall: Secondary infusion backs up into primary container.
FDA root cause: Other
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.
Quantity in commerce: 2.5 million for all products
Distribution: Nationwide and Canada.
Product codes and lots: Lot numbers: 60888186 exp 9/11 and 60869008 exp 6/11

Product code FPA

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)