• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CVS PHARMACY, INC. CVS HEAVY DUTY ANTIBACTERIAL BANDAGES; TAPE AND BANDAGE, ADHESIVE

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

CVS PHARMACY, INC. CVS HEAVY DUTY ANTIBACTERIAL BANDAGES; TAPE AND BANDAGE, ADHESIVE Back to Search Results
Model Number HEAVY DUTY ANTIBACTERIAL BANDAGES 875956
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Chemical Exposure (2570); Partial thickness (Second Degree) Burn (2694)
Event Date 01/17/2022
Event Type  Injury  
Event Description
On (b)(6) 2022 i used a (b)(6) heavy duty antibacterial bandage to cover a cut.Later in the day i had second degree chemical burns.As of (b)(6) 2022 the area is almost healed.Photos at (b)(6).Fda safety report id # (b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
CVS HEAVY DUTY ANTIBACTERIAL BANDAGES
Type of Device
TAPE AND BANDAGE, ADHESIVE
Manufacturer (Section D)
CVS PHARMACY, INC.
one cvs drive
mail code 200qa
woonsocket RI 02895
MDR Report Key13599883
MDR Text Key286261114
Report NumberMW5107697
Device Sequence Number1
Product Code KGX
UDI-Device Identifier5042826471
UDI-Public5042826471
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 02/18/2022
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 Model NumberHEAVY DUTY ANTIBACTERIAL BANDAGES 875956
Device Lot Number00139136
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received02/24/2022
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age69 YR
Patient SexMale
Patient Weight86 KG
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-