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Terminated

Line Powered RePak, Model Number 1785S

FDA Recall Z-0931-03 · Posted 2003-06-17

Recalling FirmRehabilicare
Recall StatusTerminated
Product CodeGZJ
Date Initiated2003-05-23
Date Terminated2004-07-02
Product Quantity618 Line Powered RePaks

Reason for Recall

If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.

Firm Action

Recall letters dated May 21, 2003 requested that consignees return the product and a response form to the firm. Distributors were requested to recall the product from their customers.

Root Cause

Other

Distribution Pattern

Nationwide in the United States

Official Source

View FDA Recall →

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

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