Devices

Device Recall Dafilon Suture

Model / Serial
Lot Numbers: 1-6375 1-8473 1-8433 1-9384 110054 110055
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
Yes
Distribution
Distributed in the states of IL, NY, GA, and RI.
Product Description
Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the box states the product is sterile, packaged in a cassette holding 12 sutures
Manufacturer
Aesculap, Inc.
1 Event
- Recall of Device Recall Dafilon Suture

Manufacturer

Aesculap, Inc.

Manufacturer Address
Aesculap, Inc., 3773 Corporate Pkwy, Center Valley PA 18034-8217
Manufacturer Parent Company (2017)
Ludwig G. Braun Gmbh U. Co. Kg
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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