FDA Medical Device Recalls (openFDA)
Boehringer Laboratories, Inc.: Boehringer Suction Regulator Model number 3704
- Recall number
- Z-0155-06
- Recalling firm
- Boehringer Laboratories, Inc.
- Product
- Boehringer Suction Regulator Model number 3704
- Status
- Terminated
- Initiated
- 2005-08-01
- Posted
- 2005-11-17
- Terminated
- 2005-11-16
- Reason
- Condition exists that prevents complete shutoff of the valve
- Root cause
- Other
- Action
- The recalling firm telephoned their customers on 7/25/05 to inform them of the problem, request the return of the recalled product, and inform them that replacement products were being shipped
- Quantity
- 1829 units
- Distribution
- The products were shipped to hospitals AZ, AK, CA, FL, LA, MI, MO, NC, NJ, OR, PA, SC, UT, VA, and WA.
- Lot, serial or model codes
- Lot numbers 05F and 05G
- 510(k) numbers
- ["K853095"]
- PMA numbers
- not on file
- Product code
- KDP
- Firm FEI
- 2518417
- Firm city
- Norristown
- 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