Dufner Instrumente GmbH Fohrenstr. 9 Tuttlingen Germany 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Dufner Instrumente GmbH Fohrenstr. 9 Tuttlingen Germany
Lot Codes / Batch Numbers
Lot Numbers: 8170368 and 8180673
Products Sold
Lot Numbers: 8170368 and 8180673
Dufner Instrumente GmbH Fohrenstr. 9 Tuttlingen Germany is recalling DUFNER Instrumente GmbH-De Bakey Slim Needleholder- intended to hold a suturing needle for closing w due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
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 d.moehrle@dufner-tuttlingen.de. 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,
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL
Page updated: Jan 10, 2026