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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 1 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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

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Sources and updates

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