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Terminated

Centurion brand CirClamp with 1.1 cm bell, sterile, single use; product 310.

FDA Recall Z-0837-05 · Posted 2005-05-12

Recall StatusTerminated
Product CodeHFX
Date Initiated2005-04-12
Date Terminated2005-09-08
Product Quantity1572

Reason for Recall

Not labeled as reprocessed, when this lot has been reprocessed.

Firm Action

Consignees were notified to return the product via letter dated 4/12/05.

Root Cause

Other

Distribution Pattern

Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

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

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