Z-0156-06

Boehringer Suction Regulator Model number 3704D3

Name: Z-0156-06 Boehringer Suction Regulator Model number 3704D3
Creator: Boehringer Laboratories, Inc.
Published: 2005-08-01
License: https://open.fda.gov/license/

Boehringer Laboratories, LLC / initiated 2005-08-01 / Terminated

FDA source

Boehringer Laboratories, Inc. began a recall of Boehringer Suction Regulator Model number 3704D3 on 2005-08-01. The reason FDA records is "Condition exists that prevents complete shutoff of the valve". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0156-06
Status: Terminated
Initiated: 2005-08-01
Posted: 2005-11-17
Terminated: 2005-11-16
Recalling firm: Boehringer Laboratories, LLC
Product: Boehringer Suction Regulator Model number 3704D3
Product code: KDP Regulator, Vacuum
Reason for recall: Condition exists that prevents complete shutoff of the valve
FDA 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 in commerce: 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.
Product codes and lots: Lot number 05F

Product code KDP

K853095Class IIBoehringer Laboratories Suction IntermittorBoehringer Laboratories / cleared 1985-08-23

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)