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Terminated

Triton MP-1 Traction Unit

FDA Recall Z-1215-03 · Posted 2003-09-11

Recalling FirmChattanooga Corp.
Recall StatusTerminated
Product CodeINW
Date Initiated2003-05-30
Date Terminated2004-05-07
Product Quantity96

Reason for Recall

Product contains an improper bracket for the transducer.

Firm Action

Recall notification was initiated by telephone on 05/30/2003 to the domestic accounts and via email to the foreign accounts.

Root Cause

Other

Distribution Pattern

Nationwide. TX, CO, MD, VA, FL, PA, NJ, NY, IN, OH, MI, MO, AL, NV, IL, CA, NM, AR, LA, NE, WA, NC, A, NH, and OK

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K801643TRITONChattanooga Group, Inc. · 1980-07-28

Official Source

View FDA Recall →

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

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