FDA Medical Device Recalls (openFDA)
B. Braun Medical, Inc.: Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets.
- Recall number
- Z-0819-2007
- Recalling firm
- B. Braun Medical, Inc.
- Product
- Horizon Pump Metriset Burette Set. The product is shipped in cases containing 20 sets.
- Status
- Terminated
- Initiated
- 2007-04-18
- Posted
- 2007-05-31
- Terminated
- 2008-04-22
- Reason
- Secondary infusion backs up into primary container.
- 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
- 2.5 million for all products
- Distribution
- Nationwide and Canada.
- Lot, serial or model codes
- Lot numbers: 60888186 exp 9/11 and 60869008 exp 6/11
- 510(k) numbers
- ["K904518","K955585"]
- PMA numbers
- not on file
- Product code
- FPA
- Firm FEI
- 2523676
- Firm city
- Allentown
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28