STERI-STRIP WOUND CLOSURES (REINFORCED) R1546

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2010-02-15 for STERI-STRIP WOUND CLOSURES (REINFORCED) R1546 manufactured by 3m Health Care.

Event Text Entries

[16093791] Product labeling states the expected aes with product use in the warning section shown below. Warnings: the development of postoperative edema may cause skin shearing, skin blistering, or loss of tape adhesion to occur at either end of the strip. Application of any surgical tape or adhesive skin closure may result in skin stripping upon removal. As with all adhesive products applied to the skin, a small percentage of individuals may experience hypopigmentation or hyperpigmentation, following removal. Occasional cases of mild acne and folliculitis have been observed in testing on healthy volunteers.
Patient Sequence No: 1, Text Type: N, H10


[16164167] Patient (who is a nurse) reported developing 2 big blisters and many, raised, red, smaller blisters covering the entire area under the strips and beyond, following wrist surgery. Compound benzoin tincture was used with the steri-strips. Patient was treated with silvadene and 2 doses of levaquin.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2110898-2010-00019
MDR Report Key1612559
Report Source05
Date Received2010-02-15
Date of Report2010-02-10
Date of Event2010-02-09
Date Mfgr Received2010-02-10
Date Added to Maude2010-03-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactKAREN RITTLE, MANAGER
Manufacturer Street275-5W-06
Manufacturer CityST. PAUL MN 551441000
Manufacturer CountryUS
Manufacturer Postal551441000
Manufacturer Phone6517330074
Manufacturer G13M HEALTH CARE PLANT- BROOKINGS
Manufacturer CityBROOKINGS SD
Manufacturer CountryUS
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTERI-STRIP WOUND CLOSURES (REINFORCED)
Generic NameNA
Product CodeFPX
Date Received2010-02-15
Catalog NumberR1546
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
Manufacturer3M HEALTH CARE
Manufacturer AddressST. PAUL MN US


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2010-02-15

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