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Terminated

SSCOR Suction Device Model 2310BV

FDA Recall Z-0411-05 · Posted 2005-01-27

Recalling FirmS S C O R Inc
Recall StatusTerminated
Product CodeBTA
Date Initiated2005-01-06
Date Terminated2011-06-13
Product Quantity39

Reason for Recall

Reports from medical professionals that SSCOR suction device has not performed as intended. Firm's investigation disclosed that the condition in questions is caused by cracked regulators that result in inadequate suction.

Firm Action

SSCOR Powered Suction Device not performing as intended.

Root Cause

Other

Distribution Pattern

CA, FL, IA, IL, IN, KY, MO, NC, NJ, NY, OH, France, New Zealand, Singapore, United Kingdom

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K945929S-SCORT(R)DUET MODEL 2014 PORTABLE SUCTION PUMPSscor · 1994-12-22

Official Source

View FDA Recall →

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

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