Z-1018-2007

Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123

Name: Z-1018-2007 Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123
Creator: Teleflex Creek Dr
Published: 2007-06-06
License: https://open.fda.gov/license/

Teleflex Medical / initiated 2007-06-06 / Terminated

FDA source

Teleflex Creek Dr began a recall of Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123 on 2007-06-06. The reason FDA records is "Suture Diameter/Strength specification failure: The products may not meet their final specifications for suture diameter and/or strength which could lead to premature breakage". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1018-2007
Status: Terminated
Initiated: 2007-06-06
Posted: 2007-07-17
Terminated: 2008-03-14
Recalling firm: Teleflex Medical
Product: Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123
Product code: GAM Suture, Absorbable, Synthetic, Polyglycolic Acid
Reason for recall: Suture Diameter/Strength specification failure: The products may not meet their final specifications for suture diameter and/or strength which could lead to premature breakage.
FDA root cause: Other
Action: Consignees were notified by letter on/about 06/07/2007. They were advised to cease use, remove and quarantine all affected product immediately. Affected products are to be returned to Teleflex Medical. An Acknowledgement & Stock form was included to be completed and returned via fax to Teleflex Medical.
Quantity in commerce: 1920 units total for all types of sutures
Distribution: Worldwide-, USA including states of CO, FL, IL, IN, MA, and OH, and Countries of Canada, France and Germany
Product codes and lots: Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123, Lot #35089.

Product code GAM

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)