3M™ Micropore™ 1530-0Recalls & reported problems
3m Company · 3M™ Micropore™ Tape, ¸ in X 10 yards, 24 Rolls/Carton, 10 Cartons/Case, 1530-0 · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387005086), received between Dec 5, 2018 and Dec 5, 2018 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Itching Sensation1
- Skin Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 5, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A FEMALE CUSTOMER REPORTED SHE UNDERWENT A RECENT MTP JOINT FUSION SURGERY. THE WOMAN INITIALLY APPLIED A WATERPROOF BANDAGE OVER THE WOUND SITE. PER THE RECOMMENDATION OF A CHEMIST, THE WOMAN SWITCHED TO APPLY THE REFERENCED TAPE OVER THE SITE ON (B)(6) 2018. THE TAPE WAS WORN FOR A HALF DAY. THE WOMAN ALLEGED SHE BEGAN TO EXPERIENCE DISCOMFORT. THE TAPE WAS REMOVED. SHE ALLEGED THE SKIN THAT CAME IN CONTACT WITH THE TAPE WAS RED, SORE, ITCHY AND "BURN-LIKE". THE WOMAN REPORTED SHE USED UNSPECIFIED ANTIHISTAMINES, ANTISEPTIC CREAM AND SPRAY FOR THREE DAYS TO TREAT THE AFFECTED AREA. SHE REPORTED THE INITIAL TREATMENT WAS INEFFECTIVE. ON (B)(6) 2018, THE WOMAN REPORTED THE AFFECTED AREA WAS WORSENING. SHE ALLEGED THE AFFECTED AREA STUNG AND ITCHED. THE WOMAN REPORTED HER GP ADVISED SHE EXPERIENCED AN ALLERGIC REACTION. THE DOCTOR INSTRUCTED THE WOMAN TO TAKE AN UNSPECIFIED ANTIHISTAMINE AND APPLY DERMA CREAM. THE DOCTOR ALSO PROVIDED THE WOMAN WITH A PRESCRIPTION FOR "ELACON" CREAM TO USE IF THE DERMA CREAM WAS INEFFECTIVE. SHE ALLEGED EXPERIENCING DISCOMFORT DUE TO HER FOOT SWELLING FROM THE RECENT SURGERY COMBINED WITH THE ALLERGIC REACTION. THE WOMAN REPORTED ALLERGIES TO MANY C
Patient problems: Itching Sensation; Skin Irritation
MAUDE report 8134819 ↗
Other Tape and bandage, adhesive devices
- IV3000-1-HAND 10X12CM-CARTON OF 50 66024008Smith & Nephew Medical Limited · Tape And Bandage, Adhesive62 reports
- CURAD NON25600QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall2 reports
- IV3000-1-HAND 6X7CM-CARTON OF 100 66024007Smith & Nephew Medical Limited · Tape And Bandage, Adhesive52 reports
- CURAD NON25650QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall1 report
- 3M™ 1500U3m Company · Tape and bandage, adhesive1 recall1 report
- Lucky Super Soft Bandages in differenet sizeDelta Brands Inc. · Tape And Bandage, Adhesive1 recall0 reports
- 3M™ Durapore™ 1538-1183M Deutschland GmbH · Tape and bandage, adhesive1 recall0 reports
- CURAD NON256133QSMedline Industries, Inc. · Tape and bandage, adhesive1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page