FDA Medical Device Recalls (openFDA)
Boehringer Laboratories Inc: Boheringer Suction Regulator Model 7702L, Lot number 04D Boehinger Replacement Gauge, Model 9071, Lot number 200405.
- Recall number
- Z-1231-04
- Recalling firm
- Boehringer Laboratories Inc
- Product
- Boheringer Suction Regulator Model 7702L, Lot number 04D Boehinger Replacement Gauge, Model 9071, Lot number 200405.
- Status
- Terminated
- Initiated
- 2004-05-19
- Posted
- 2004-07-20
- Terminated
- 2004-09-14
- Reason
- The suction regulator incorporates a gauge for the verification of suction levels. The particular lot of gauges used in the production of the regulators exhibits a potential to develop a leak and cause the delivered suction to be inaccurate.
- Root cause
- Other
- Action
- All direct accounts were contacted by the recalling firm''s Customer Service Representative to determine the location of the affected product. The CSR arrange for replacement proudct.
- Quantity
- 56 units
- Distribution
- The recalled product was distributed to the following states: AL, FL, MA, MI, OR, PA, TN,
- Lot, serial or model codes
- Regulator Model 7702L, Lot Number 04D
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- GCX
- 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