Cultura™ 00884450495834Recalls & reported problems
Merit Medical Systems, Inc. · Class 1
All models of Cultura (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884450495834), received between Sep 14, 2020 and Sep 30, 2020 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2020Fracture; Fracture
THE ACCOUNT ALLEGES THAT A PATIENT WAS ADMITTED TO THE ED WITH LOWER BACK PAIN RADIATING INTO HIS UPPER LEGS BILATERALLY. THE PATIENT HAS A HISTORY OF CHRONIC THORACIC AND LUMBAR PAIN, ASSOCIATED VERTEBRAL HERNIATIONS, AND METHAMPHETAMINE INTRAVENOUS DRUG USE. THE PATIENT WAS TRANSFERRED FOR FURTHER PAIN EVALUATION AND INFECTIOUS ETIOLOGY / DEGENERATIVE CHANGES WITH LUMBAR RADICULOPATHY. PRIOR TO TRANSFER, COVID19 TESTING WAS ORDERED. AN RN PERFORMED COVID19 NASOPHARYNGEAL SWAB WITHIN THE LEFT ANTERIOR NARES. THE SWAB BROKE 4.5 CM FROM RED LINE WHERE SWAB NARROWS. THE PATIENT IMMEDIATELY SNIFFED, AND THE SWAB DISAPPEARED INTO NASOPHARYNGEAL CAVITY. THE EMERGENCY ROOM PHYSICIAN WAS NOTIFIED IMMEDIATELY. THE PATIENT WAS INSTRUCTED TO BLOW HIS NOSE IN ATTEMPTS TO EXPEL THE DETACHED TIP WITH NO SUCCESS. A NASAL SPECULUM WAS THEN USED TO TRY AND LOCATE THE DETACHED TIP WITH NO SUCCESS. THE PHYSICIAN WAS NOT ABLE TO LOCATE OR VISUALIZE THE SWAB. AN X-RAY WAS COMPLETED WITH NO IDENTIFICATION OF THE SWAB WITHIN THE NASOPHARYNGEAL CAVITY. AN ENT WAS CONSULTED, AND AFRIN WAS ADMINISTRATED FOR THE PATIENT'S CONGESTION. TREATMENT INITIATED WITHOUT RETRIEVAL OF THE SWAB AS WELL. THE PATIENT DEM
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10610672 ↗MalfunctionSep 14, 2020Break
THE PATIENT ADMITTED TO THE ED WITH LOWER BACK PAIN RADIATING INTO BILATERAL UPPER LEGS. THE PATIENT HAS A HISTORY OF CHRONIC THORACIC AND LUMBAR PAIN AND ASSOCIATED DISC HERNIATIONS, AS WELL METHAMPHETAMINE IVDU. FOLLOWING WORK-UP, PLAN WAS MADE TO TRANSFER FOR FURTHER EVALUATION OF PAIN AND DETERMINE IF INFECTIOUS ETIOLOGY VS DEGENERATIVE CHANGES WITH RADICULOPATHY. PRIOR TO TRANSFER, COVID TESTING WAS ORDERED. RN PERFORMED COVID 19 NASOPHARYNGEAL SWAB IN LEFT NOSTRIL. THE SWAB BROKE 4.5CM FROM RED LINE WHERE SWAB NARROWS. THE PT IMMEDIATELY SNIFFED AND SWAB DISAPPEARED INTO NARE. THE ED MD WAS NOTIFIED IMMEDIATELY. THE PT BLEW HIS NOSE, WITH NO RETURN OF THE SWAB. A NASAL SPECULUM WAS USED IN ATTEMPT TO LOCATE AND WAS UNABLE TO LOCATE/VISUALIZE THE SWAB. X-RAY COMPLETED WITH NO VISUALIZATION. ENT WAS CONSULTED AND RECOMMENDED AFRIN ADMINISTRATION. TREATMENT INITIATED WITHOUT RETRIEVAL OF THE SWAB. THE PATIENT DEMONSTRATED NO RESPIRATORY DISTRESS - HIS ONLY COMPLAINT WAS CONGESTION. THE PATIENT WAS TRANSFERRED FOR FURTHER EVALUATION OF THE LOW BACK PAIN, WITH PLAN FOR ENT TO EVALUATE PATIENT. NASAL ENDOSCOPY WAS PERFORMED THE FOLLOWING DAY AFTER ADMINISTRATION OF LIDOCAINE/PHENYL
Patient problems: Foreign Body In Patient
MAUDE report 10527436 ↗
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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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