Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123
Lot Codes / Batch Numbers
Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123, Lot #35089.
Products Sold
Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123, Lot #35089.
A medical device manufacturer is recalling Nonabsorbable Polypropylene Synthetic Suture-Deklene, DEK BL MF 0 TC-43 2N 48, Catalog #833-123 due to Suture Diameter/Strength specification failure: The products may not meet their final specifications for suture diameter and/or strength which could l. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
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
CO, FL, IL, IN, MA, OH
Page updated: Jan 10, 2026