Devices

Device Recall Sterilux

Model / Serial
Item # 56910000 (Sterilux): 102147399, 102250396, 200105390, 200206394
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide distribution: USA including states of: AZ, CA, FL, GA, KY, MO, MS, NC, PA, SC, TN, TX, and VA.
Product Description
Hartmann Sterilux Ref 56910000 Sterile Premium gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges || For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing
Manufacturer
Hartmann USA, Inc
1 Event
- Recall of Device Recall Sterilux

Manufacturer

Hartmann USA, Inc

Manufacturer Address
Hartmann USA, Inc, 481 Lakeshore Pkwy, Rock Hill SC 29730-4205
Manufacturer Parent Company (2017)
Schwenk Limes Gmbh & 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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