MAUDE Adverse Event Report: JOHNSON+JOHNSON CONSUMER, INC. BAND-AID; TAPE AND BANDAGE, ADHESIVE

Patient Problems Hypersensitivity/Allergic reaction (1907); Unspecified Tissue Injury (4559)

Event Date 08/20/2023

Event Type  Injury  

Event Description

I purchased band-aid true-stay sheer 80 assorted sizes by johnson+johnson.The product did not include the list of harmful chemicals and allergens and was marketed as safe for use.Patent #(b)(4).I had a severe reaction to the secret use of nickel.I am deathly allergic and almost lost my finger after 10-mins of exposure.Require every single product advertised as a health product to include hazardous chemicals, common allergens, and poisonous substances.I should not almost loose my finger from "allergy safe" branded band-aids.Shame on you for allowing this intentional disregard for the safety of humanity.

• Brand Name: BAND-AID
• Type of Device: TAPE AND BANDAGE, ADHESIVE
• Manufacturer (Section D): JOHNSON+JOHNSON CONSUMER, INC.
• MDR Report Key: 17604639
• MDR Text Key: 321886243
• Report Number: MW5144875
• Device Sequence Number: 1
• Product Code: KGX
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Unknown
• Type of Report: Initial
• Report Date: 08/20/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Was Device Available for Evaluation?: Yes
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 08/22/2023
• Patient Sequence Number: 1
• Patient Outcome(s): Life Threatening; Other; Required Intervention
• Patient Age: 29 YR
• Patient Ethnicity: Non Hispanic
• Patient Race: White