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Terminated

VSP Shock Module (as part of a prosthetic foot).

FDA Recall Z-1083-04 · Posted 2004-07-20

Recalling FirmOssur North America Inc
Recall StatusTerminated
Product CodeISH
Date Initiated2004-06-15
Date Terminated2005-06-17
Product Quantity37

Reason for Recall

Flawed shock module might cause breakage causing patient to fall.

Firm Action

Firm will be contacting customers and patients to replace the defective components. Contact will be made by mail and by phone.

Root Cause

Other

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

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

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