Boehringer Suction Regulator Model number 3704D3
FDA Recall Z-0156-06 · Posted 2005-11-17
Recalling FirmBoehringer Laboratories, Inc.
Recall StatusTerminated
Product CodeKDP
Date Initiated2005-08-01
Date Terminated2005-11-16
Product Quantity1829 units
Reason for Recall
Condition exists that prevents complete shutoff of the valve
Firm 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
Root Cause
Other
Distribution Pattern
The products were shipped to hospitals AZ, AK, CA, FL, LA, MI, MO, NC, NJ, OR, PA, SC, UT, VA, and WA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.