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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: JOHNSON & JOHNSON CONSUMER INC BAND AID BRAND BREATHABLE BANDAGES AP 1361CAP; TAPE AND BANDAGE, ADHESIVE

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JOHNSON & JOHNSON CONSUMER INC BAND AID BRAND BREATHABLE BANDAGES AP 1361CAP; TAPE AND BANDAGE, ADHESIVE Back to Search Results
Model Number 6916999000713
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Erythema (1840); Itching Sensation (1943); Discomfort (2330)
Event Date 03/17/2021
Event Type  Injury  
Manufacturer Narrative
Device was used for treatment, not diagnosis.Patient identifier, weight, and ethnicity and race were not provided for reporting.This report is for band-aid breathable 16ct ap (b)(4).Device is not distributed in the united states.Band-aid breathable 16ct ap (b)(4) is similar to device marketed in the usa (bab sheer 1inx3in usa 38137004770 8137004770usa 8137004770usa).Udi #: (b)(4).Upc #: 6916999215513.Lot #: 200413 1813.Exp: na.Device is not expected to be returned for manufacturer review/investigation.Device is not distributed in the united states, but is similar to device marketed in the usa (band-aid breathable 16ct ap (b)(4).Device history records review was completed.No non-conformance reports were generated during production.Review of the device history records showed that there were no issues during the manufacture of the product that would contribute to this complaint condition and product was manufactured per specification.The product was manufactured on april 13, 2020.This is 2 of 2 med-watches being submitted, as it was unknown which band-aid product was involved in this event.See medwatch 1000599868-2021-00004.The same patient is represented in each medwatch.If information is obtained that was not available for this initial medwatch, an additional follow-up medwatch will be filed as appropriate.
 
Event Description
Consumer reported an event for pediatric consumer ((b)(6)old) using band-aid breathable ap for a skin scratch.The consumer purchased a bandage from the hospital on (b)(6) 2021 and took it home and applied it to the skin scratch of the consumer¿s right hand.Around noon time of (b)(6) 2021, the pediatric consumer had developed itchy skin and stopped using the bandage.Consumer visited a hospital for treatment.The consumer showed mild skin redness at the scratch site.The bandage was discontinued, and the patient and was given fluocinonide cream (to prevent infection and to accelerate healing) for application after examination.The consumer returned home and was told to keep it under observation.The consumer was followed up for discomfort.This is 2 of 2 med-watches being submitted, as it was unknown which band-aid product was involved in this event.See medwatch 1000599868-2021-00004.The same patient is represented in each medwatch.
 
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Brand Name
BAND AID BRAND BREATHABLE BANDAGES AP 1361CAP
Type of Device
TAPE AND BANDAGE, ADHESIVE
Manufacturer (Section D)
JOHNSON & JOHNSON CONSUMER INC
199 grandview rd
skillman NJ 08558 9418
Manufacturer (Section G)
SHANGHAI JOHNSON & JOHNSON LTD.
120 nan ya road
minhang, shanghai
CH  
Manufacturer Contact
laurie rauco
199 grandview rd
skillman, NJ 08558-9418
2152734905
MDR Report Key11729517
MDR Text Key263169626
Report Number1000599868-2021-00005
Device Sequence Number1
Product Code KGX
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer,foreign
Type of Report Initial
Report Date 03/30/2021
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? No
Device Operator Lay User/Patient
Device Model Number6916999000713
Device Lot Number200413 1813
Was Device Available for Evaluation? No
Event Location Other
Initial Date Manufacturer Received 03/30/2021
Initial Date FDA Received04/26/2021
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured04/13/2020
Is the Device Single Use? Yes
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age06 YR
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