International Medical Devices Database

Manufacturer Address
Smith And Nephew, Inc. Wound Management Division, 11775 Starkey Rd, Largo FL 33773
Source
USFDA
1 Event
- Recall of Acticoat

One device in the database

Acticoat

Model / Serial
021022A, 021023A, 021118A, 030106A, 030107A
Product Classification
General and Plastic Surgery Devices
Distribution
The recalled devices were distributed to 81 direct wholesalers or medical facilities nationwide. There were no direct international or government/military accounts.
Product Description
Acticoat* Moisture Control Dressing, Product Code 20211, Distributed by Smith & Nephew, Inc., Wound Management Division, 11775 Starkey Road, Largo, FL 33773

One manufacturer with a similar name

Learn more about the data here

Smith And Nephew, Inc. Wound Management Division

Manufacturer Address
Smith And Nephew, Inc. Wound Management Division, 11775 Starkey Road, Largo FL 33773-4727
Manufacturer Parent Company (2017)
Smith & Nephew plc
Source
USFDA

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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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