MEDLINE MSC4226EPRecalls & reported problems
Medline Industries, Inc. · STICKRIGHT, 6" X 2 YD · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10197344102785), received between Jun 29, 2026 and Jun 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Adhesive Too Strong” (6 reports).
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.
Reports received per month
Most reported problems
Device problems
- Adhesive Too Strong6
- Patient Device Interaction Problem3
Patient problems
- Blister6
- Skin Tears6
- Burning Sensation5
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 30, 2026Patient Device Interaction Problem; Adhesive Too Strong
ACCORDING TO THE CUSTOMER, ON (B)(6) 2026 UPON REMOVAL OF THE TAPE THE PATIENT EXPERIENCED A "BURNING SENSATION, BLISTER FORMATION, AND/OR SKIN TEARING". THE CUSTOMER REPORTED THAT THE PATIENT REQUIRED A WOUND CARE CONSULT TO MANAGE THE INJURY.
Patient problems: Blister; Burning Sensation; Skin Tears
MAUDE report 25672450 ↗MalfunctionJun 30, 2026Patient Device Interaction Problem; Adhesive Too Strong
ACCORDING TO THE CUSTOMER, ON (B)(6) 2026, UPON REMOVAL OF THE TAPE THE PATIENT EXPERIENCED A "BURNING SENSATION, BLISTER FORMATION, AND/OR SKIN TEARING". THE CUSTOMER REPORTED THAT THE PATIENT REQUIRED A WOUND CARE CONSULT TO MANAGE THE INJURY AND "AND ONE HOME WOUND CARE TREATMENT".
Patient problems: Blister; Burning Sensation; Skin Tears
MAUDE report 25670272 ↗MalfunctionJun 30, 2026Adhesive Too Strong
ACCORDING TO THE CUSTOMER, ON (B)(6) 2026, UPON REMOVAL OF THE TAPE THE PATIENT EXPERIENCED A "BURNING SENSATION, BLISTER FORMATION, AND/OR SKIN TEARING". NO ADDITIONAL DETAILS ARE AVAILABLE RELATED TO THE CUSTOMER REPORTED ISSUE.
Patient problems: Blister; Burning Sensation; Skin Inflammation/ Irritation; Skin Tears
MAUDE report 25670057 ↗MalfunctionJun 30, 2026Adhesive Too Strong
ACCORDING TO THE CUSTOMER, ON (B)(6) 2026 UPON REMOVAL OF THE TAPE THE PATIENT EXPERIENCED A "BURNING SENSATION, BLISTER FORMATION, AND/OR SKIN TEARING".
Patient problems: Blister; Burning Sensation; Skin Tears
MAUDE report 25666033 ↗MalfunctionJun 30, 2026Adhesive Too Strong
ACCORDING TO THE CUSTOMER, ON (B)(6) 2026 UPON REMOVAL OF THE TAPE THE PATIENT EXPERIENCED A "BURNING SENSATION, BLISTER FORMATION, AND/OR SKIN TEARING".
Patient problems: Blister; Burning Sensation; Skin Tears
MAUDE report 25664220 ↗MalfunctionJun 29, 2026Patient Device Interaction Problem; Adhesive Too Strong
BURNING SENSATION, BLISTER FORMATION AND/OR SKIN TEARING.
Patient problems: Blister; Skin Tears
MAUDE report 25653800 ↗
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.
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