Devices

Device Recall Nonabsorbable Surgical Suture

Model / Serial
Product Code 1154654 - Lot 02K0801212
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
Yes
Distribution
Worldwide Distribution -- USA, including the states of AL, CA, FL, GA, IL, IN, KS, LA, ME, MA, MI, MN, MS, MO, NV, NJ, NM, NY, OH, PA, RI, SC, TN, TX, UT, VA, WV, and WI; and countries of Canada, Germany, and Ireland.
Product Description
Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel. || Indicated for use in soft tissue approximation.
Manufacturer
Teleflex Medical
1 Event
- Recall of Device Recall Nonabsorbable Surgical Suture

Manufacturer

Teleflex Medical

Manufacturer Address
Teleflex Medical, 4024 Stirrup Creek Dr, Durham NC 27703-9000
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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