Shiley 8888247015Recalls & reported problems
Covidien LP · Nasopharyngeal Airway · Class 1
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 60884521133070), received between Jul 30, 2025 and Jul 30, 2025 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Defective Component” (7 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Defective Component7
Patient problems
- No Clinical Signs, Symptoms or Conditions7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668269 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668262 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668242 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668218 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668201 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668156 ↗MalfunctionJul 30, 2025Defective Component; Defective Component
IT WAS REPORTED THAT DURING INSPECTION, SEVEN OUT OF TEN NASOPHARYNGEAL TUBES TOTAL LENGTH WERE FOUND TO BE OUTSIDE THE LIMITS OF DETECTION BASED ON PRODUCT SPECIFICATIONS. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22668154 ↗
Other AIRWAY, NASOPHARYNGEAL devices
- RUSCH IPN042923Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL5 reports
- RUSCH IPN042918Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042921Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Mallinckrodt 8888247064Covidien LP · AIRWAY, NASOPHARYNGEAL2 reports
- RUSCH IPN042925Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL2 reports
- Curaplex 2021-15028Bound Tree Medical, LLC · AIRWAY, NASOPHARYNGEAL1 report
- RUSCH IPN042213Teleflex Incorporated · AIRWAY, NASOPHARYNGEAL1 report
- SunMed 1-5075-34Sunmed, LLC · AIRWAY, NASOPHARYNGEAL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.