Devices

Device Recall Johnson & Johnson BANDAID Brand First Aid Products SECUREFLEX Wrap

Model / Serial
111615000 381371161508 103813711615050000
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationally
Product Description
Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in)
Manufacturer
Johnson & Johnson Consumer, Inc.
1 Event
- Recall of Device Recall Johnson & Johnson BANDAID Brand First Aid Products SECUREFLEX Wrap

Manufacturer

Johnson & Johnson Consumer, Inc.

Manufacturer Address
Johnson & Johnson Consumer, Inc., 199 Grandview Rd, Skillman NJ 08558-1311
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Johnson & Johnson BANDAID Brand First Aid Products SECUREFLEX Wrap

Model / Serial
111615100 381371161515 103813711615120000
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationally
Product Description
Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 3in)
Manufacturer
Johnson & Johnson Consumer, Inc.

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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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