Bard PTFE FeltRecalls & reported problems across all models
Bard Peripheral Vascular, Inc. · 5 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 71
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 0
We found 5 models of Bard PTFE Felt by Bard Peripheral Vascular, Inc. in the FDA's device registry (GUDID). Together they are named in 71 adverse event reports in the FDA's MAUDE database, received between Jan 19, 2018 and Nov 29, 2025 — classified as 1 injury, 70 malfunctions.
The most frequently reported specific device problem is “Incomplete or Missing Packaging” (63 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Bard PTFE Felt problems
Device problems
- Incomplete or Missing Packaging63
- Missing Information9
- Device Contamination with Chemical or Other Material3
- Tear, Rip or Hole in Device Packaging2
- Adverse Event Without Identified Device or Use Problem1
- Contamination1
- Device Handling Problem1
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions66
- No Patient Involvement3
- No Consequences Or Impact To Patient1
- Pain1
- Unspecified Infection1
Bard PTFE Felt models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Bard® PTFE Felt 007975PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE28 reports
- Bard® PTFE Felt 007973PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE22 reports
- Bard® PTFE Felt 007976PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE14 reports
- Bard® PTFE Felt 007837PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE5 reports
- Bard® PTFE Felt 007836PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE2 reports
Recent Bard PTFE Felt adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675642 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675641 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE IS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675640 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675639 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675638 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675633 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675628 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. IT WAS REPORTED THAT DURING TO A SURGICAL PLACEMENT PROCEDURE USING THE PTFE FELT DEVICE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675627 ↗MalfunctionNov 29, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, A CUSTOMER REPORTED NOT RECEIVING THE PATIENT INFORMATION CARD (PIC). THERE NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23675626 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23670162 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23670098 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23670092 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING THE PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD (PIC) WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23669674 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING THE PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD (PIC) WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23669537 ↗MalfunctionNov 28, 2025Incomplete or Missing Packaging; Incomplete or Missing Packaging
A PATIENT UNDERWENT A SURGICAL PLACEMENT PROCEDURE USING PTFE FELT DEVICE. DURING THE PROCEDURE, IT WAS REPORTED THAT THE PATIENT INFORMATION CARD WAS NOT RECEIVED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23669536 ↗
Other Bard Peripheral Vascular, Inc. products
- MAX-CORE11 models · 8,845 reports · 1 recall
- DENALI Vena Cava Filter2 models · 1,021 reports
- MAGNUM19 models · 571 reports · 1 recall
- Conquest32 models · 560 reports
- Ultraverse RX56 models · 536 reports
- Fluency Endovascular Stent Graft51 models · 532 reports
- Atlas Gold33 models · 427 reports
- Ultraverse 035 PTA Dilatation Catheter92 models · 393 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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