Boehringer Laboratories, Inc. Boehringer Suction Regulator Model number 3704 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Boehringer Suction Regulator Model number 3704
Brand
Boehringer Laboratories, Inc.
Lot Codes / Batch Numbers
Lot numbers 05F and 05G
Products Sold
Lot numbers 05F and 05G
Boehringer Laboratories, Inc. is recalling Boehringer Suction Regulator Model number 3704 due to Condition exists that prevents complete shutoff of the valve. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Condition exists that prevents complete shutoff of the valve
Recommended Action
Per FDA guidance
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
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AK, AZ, CA, FL, LA, MI, MO, NJ, NC, OR, PA, SC, UT, VA, WA
Page updated: Jan 10, 2026