No Sting Skin-Prep Prot. Spray 28ml US 66800709Recalls & reported problems
Smith & Nephew Medical Limited · No-Sting Barrier Film · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05000223469566), received between Apr 19, 2021 and Oct 14, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Fire” (1 report).
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fire1
- Off-Label Use1
Patient problems
- Blurred Vision1
- Burn(s)1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 14, 2024Off-Label Use; Off-Label Use
IT WAS REPORTED THAT THE PATIENT HAD ISSUES WITH HIS LEFT EYE AGAIN, AFTER HE MISTAKENLY SPRAYED NO-STING SKIN PREP SPRAY 28ML US IN HIS EYE. THE PATIENT SAID HE HAD A HISTORY OF RETINA REPLACEMENT 5-6 YEARS AGO, BUT HIS EYESIGHT CAME BACK. ON (B)(6) 2024, HE WAS HOSPITALIZED FOR 2 MONTHS DUE TO PSYCHIATRIC PROBLEMS. HE WAS GIVEN THIS PRODUCT DURING HIS STAY AT THE HOSPITAL, AND ACCIDENTALLY SPRAYED HIS EYES. HE COULD NOT TELL THE EXACT DATE HE STARTED USING IT, BUT HE MENTIONED IT WAS FREQUENTLY DUE TO A WOUND ON HIS STOMACH. HE WAS INFORMED THAT PRECAUTION INCLUDES TO AVOID EYE CONTACT, AND THAT IN THE CASE OF ACCIDENTAL CONTACT, HE MUST FLUSH EYES WELL WITH WATER, SINCE LOSING EYESIGHT IS NOT A COMMON SIDE EFFECT. HIS RIGHT EYE WAS STILL COVERED, AND WITH HIS LEFT EYE HE COULD SEE A LITTLE BIT. HE WAS REFERRED TO HCP. IT IS UNKNOWN HOW THE TREATMENT WAS CONTINUED. THERE IS NO FURTHER INFORMATION AVAILABLE.
Patient problems: Blurred Vision
MAUDE report 20440465 ↗InjuryApr 19, 2021Fire; Fire
IT WAS REPORTED THAT THERE WAS A SURGICAL FIRE, AND HEALTH CARE PROFESSIONAL SPRAYED THE SKIN PREP ON THE PATIENT. THE SKIN CAUGHT FIRE WHILE WAITING FOR THE PREP TO DRY. NO FURTHER INFORMATION IS KNOWN REGARDING THE AE AT THIS TIME.
Patient problems: Burn(s)
MAUDE report 11684622 ↗
Other Bandage, Liquid, Skin Protectant devices
- APLICARE APLS1106Medline Industries, Inc. · Bandage, liquid, skin protectant4 reports
- Protective Barrier Film 740013C. R. Bard, Inc. · Bandage, liquid, skin protectant2 reports
- SKIN-PREP Wipes 420400, 420471Smith & Nephew Medical Limited · Bandage, Liquid, Skin Protectant1 report
- Medline MSC1500Medline Industries, Inc. · Bandage, liquid, skin protectant1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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