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

DUFNER Instrumente GmbH-De Bakey Slim Needleholder- intended to hold a suturing needle for closing wounds during suturing and surgical procedures Reference Number: 18044-23

FDA Recall Z-2534-2020 · Posted None

Recall StatusTerminated
Product CodeFHQ
Date Initiated2020-06-03
Date Terminated2021-01-21
Product Quantity30 units

Reason for Recall

Tungsten carbide plate, which is intended to hold the sewing needle securely, can break when holding the sewing needle under pressure and result in in patient tissue injury

Firm Action

Dufner Instruments GMB issued letter dated June 3, 2020, staing reason for recall, health risk and action to take: 1. Immediately remove all products of the affected article number with the named lots fromyour warehouse or from affected instrument trays to prevent further use. 2. With this letter you will receive a confirmation form, please fill it in completely, sign it and send it back to us after receiving this information. If you do not own any affected products, please fill out the confirmation form anyway and fax it to +49 (0)7461/79419 or mail it to [email protected]. 3. Send back to us immediately all products still in stock. After receipt of the goods we will send you a credit note and clarify with you the further procedure. 4. Pass this information on to all staff in your institution, who should be informed. Please ensure that all users of the affected products within your organization and also all other affected persons receive this information through the Field Safety Notice. If products have been passed on to third parties, please also send them a copy of the Field Safety Notice or inform our contact person to contact the third parties,

Root Cause

Process control

Distribution Pattern

IL

Official Source

View FDA Recall →

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

↑