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Terminated

Boehringer Suction Regulator Model number 3704

FDA Recall Z-0155-06 · 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.

K853095BOEHRINGER LABORATORIES SUCTION INTERMITTORBoehringer Laboratories · 1985-08-23

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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