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Terminated

Corin TriFit CF SIZE 7, LATERALISED 127o, COMBINED FIXATION STEM, CEMENTLESS, REF 6961007. Hip prosthesis component.

FDA Recall Z-1851-2021 · Posted None

Recalling FirmCorin Ltd
Recall StatusTerminated
Product CodeMEH
Date Initiated2021-05-06
Date Terminated2023-07-05
Product Quantity1 unit

Reason for Recall

Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.

Firm Action

Corin initiated the recall by email on 05/06/2021 and followed with a letter on 05/07/2021 disseminated by email. The firm is seeking the return of the product.

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide distribution in the state of TX.

Official Source

View FDA Recall →

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

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