Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Centurion brand CirClamp with 1.3 cm bell, sterile, single use; product 330.

FDA Recall Z-0836-05 · Posted 2005-05-12

Recall StatusTerminated
Product CodeHFX
Date Initiated2005-04-12
Date Terminated2005-09-08
Product Quantity4078

Reason for Recall

Lot 11224 may contain a 1.1 cm clamp and bell and neither lot is labeled as reprocessed, when they have 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.

↑