Bivona 60SN025Recalls & reported problems
Icu Medical, Inc. · Class 2
All models of Bivona (469)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15021312000115), received between Apr 5, 2022 and Apr 5, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
46 other recalls cover devices cleared under the same FDA submission (K083641, K912469); they may or may not involve this specific model.
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.
Recalls naming this device
- May 29, 2024Class IOpen, Classified
Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
Z-2602-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 5, 2022Break; Break
IT WAS REPORTED THAT THE TRACH HAD BROKEN AT THE FLANGE/TUBE WHILE THE PATIENT WAS AT HOME. THE TRACH WAS IN THE PT WHEN IT BROKE. THE TRACH HAD NOT BEEN IN USE FOR VERY LONG. IT WAS BEING CLEANED AS PER MANUFACTURERS RECOMMENDATION. THE PATIENT HAS HAD THIS SIZE TRACH FOR SOME TIME AND HAS NOT HAD ISSUES WITH OTHER TRACHS. THE ISSUE WAS RESOLVED BY SWAPPING OUT THE TRACH. THERE WAS NO PATIENT INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14014244 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083641, K912469. One submission often covers many models, so check the product and lot details in each record.
- Z-2597-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: 6.0MM FLEXTEND PEDIATRIC PLUS VEE TRACH TUBE , Product Code/List Number/Item Code 60PFP60
- Z-2611-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) PEDIATRIC TRACHEOSTOMY TUBE 4.0mm TTS FLEXTEND PLUS V FLANGE , Product Code/List Number/Item Code 67PFP40; b) PEDIATRIC
- Z-2598-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) 4.0MM FLEXTEND PEDIATRIC PLUS STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60PFPS40; b) 4.5MM FLEXTEND PEDI
- Z-2600-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: 2.5MM PEDIATRIC UNCUFFED FLEXTEND PLUS TRACHEOSTOMY TUBE WITH NEONATE STRAIGHT NECKSTRAP, Product Code/List Number/Item Code
- Z-2601-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) 3.0MM FLEXTEND PEDIATRIC STANDARD STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60PFSS30; b) 3.5MM FLEXTEND
- Z-2593-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: 2.5MM UNCUFFED NEONATAL FLEXTEND PLUS TRACHEOSTOMY TUBE W/NEO STRAIGHT STRAP, Product Code/List Number/Item Code 60NFPS25
- Z-2589-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) AIRE-CUF TRACHY TUBE 6.0MM MID-RANGE , Product Code/List Number/Item Code 750160; b) AIRE-CUF TRACHY TUBE 7.0MM MID-RAN
- Z-2612-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) PEDIATRIC TRACHEOSTOMY TUBE 4.0mm TTS FLEXTEND PLUS STRAIGHT FLANGE , Product Code/List Number/Item Code 67PFPS40; b) PE
- Z-2590-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code 60N025
- Z-2610-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS PEDIATRIC TRACH TUBE , Product Code/List Number/Item Code 67P025; b) TTS PEDIATRIC TRACH TUBE , Product Code/List Nu
- Z-2608-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACHEOSTOMY TUBE 2.5mm TTS FLEXTEND V FLANGE , Product Code/List Number/Item Code 67NFP25; b) NEONATAL TRACHEO
- Z-2594-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) 3.0MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS30; b) 3.5MM FLEXTEND NEO STRAIGHT T
- Z-2591-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N030; b) NEONATAL TRACH TUBE , Product Code/List Number/Item
- Z-2588-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Code 670170; b) TTS TRACHEOSTOMY TUBE 8.0
- Z-2615-2024 · May 29, 2024 · Open, ClassifiedPORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) 2.5mm TTS CUFFED NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code 67SN025; b) 3.0mm TTS CUFFED NEONATAL T
…and 31 more.
Other Tube, tracheostomy (w/wo connector) devices
- Portex 101/860/080CZIcu Medical, Inc. · Tube, tracheostomy (w/wo connector)188 reports
- Portex 101/860/075CZIcu Medical, Inc. · Tube, tracheostomy (w/wo connector)115 reports
- Bivona 60SP040Icu Medical, Inc. · Tube, tracheostomy (w/wo connector)1 recall20 reports
- Bivona 60SP050Icu Medical, Inc. · Tube, tracheostomy (w/wo connector)1 recall13 reports
- Bivona 60P040Icu Medical, Inc. · Tube, tracheostomy (w/wo connector)1 recall12 reports
- Portex 101/860/070CZIcu Medical, Inc. · Tube, tracheostomy (w/wo connector)60 reports
- Bivona 60SP045Icu Medical, Inc. · Tube, tracheostomy (w/wo connector)1 recall8 reports
- Bivona 60SN040Icu Medical, Inc. · Tube, tracheostomy (w/wo connector)1 recall5 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 · each recall links to the FDA recall notice
- 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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