BD VeoRecalls & reported problems across all models
Becton, Dickinson and Company Inc · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 726
- Deaths reported
- 0
- Injuries reported
- 15
- Recalls
- 0
We found 5 models of BD Veo by Becton, Dickinson and Company Inc in the FDA's device registry (GUDID). Together they are named in 726 adverse event reports in the FDA's MAUDE database, received between Oct 24, 2017 and Sep 29, 2026 — classified as 15 injuries, 711 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (200 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 BD Veo problems
Device problems
- Leak/Splash200
- Device Contamination with Chemical or Other Material141
- Device Markings/Labelling Problem89
- Failure to Deliver81
- Volume Accuracy Problem60
- Defective Device40
- Break35
- Delivered as Unsterile Product17
Patient problems
- No Known Impact Or Consequence To Patient282
- No Clinical Signs, Symptoms or Conditions271
- No Consequences Or Impact To Patient120
- No Patient Involvement29
- Needle Stick/Puncture8
- No Information6
- Hyperglycemia5
- Insufficient Information5
BD Veo models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Veo 324910Syringe, piston279 reports
- BD Veo 324911Syringe, piston189 reports
- BD Veo 324909Syringe, piston152 reports
- BD Veo 324912Syringe, piston105 reports
- BD Veo 324906Syringe, piston1 report
Recent BD Veo adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937040 ↗MalfunctionSep 29, 2026Failure to Deliver
From: (b)(6) Sent: Tuesday, June 25, 2024 1:39 AM To:(b)(6) Subject: Direct Consumer 2024-06-17 Product Inquiry - Inquiry Ref: "[ ref:!00D300Y0Yr.!5008a02ZEn2J:ref ]" From: (b)(6) Sent: Tuesday, June 25, 2024 1:39 AM To: (b)(6) Subject: Direct Consumer 2024-06-17 Product Inquiry - Inquiry Ref: "[ ref:!00D300Y0Yr.!5008a02ZEn2J:ref ]" Direct Consumer 2024-06-24 Product Inquiry - Inquiry Ref:Consumer reported could not draw his insulin because he believes the needles are blocked. Lot: 3128169Catalog: 324910Date of Event: 2024-06-24Samples: No3 syringes affectedDeclined to provide address and declined replacement. Email came into Outlook but did not come into Salesforce. CLtmaik see email for Date of Event correction:Date of Event - (b)(6), 2024.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50927101 ↗MalfunctionSep 28, 2026Off-Label Use; Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916910 ↗MalfunctionSep 28, 2026Off-Label Use; Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916679 ↗MalfunctionSep 28, 2026Off-Label Use; Device Contamination with Chemical or Other Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916451 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC Lot # 3240237Catalog# 324911Date of Event unknown Sample Status Discard_________________________________________This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. Daleryn Perez 09 SEP 2026
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50912394 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC. Lot # 3240237.Catalog# 324911.Date of Event unknown.Sample Status Discard.This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. (b)(6), 09 SEP 2026.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50912333 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC Lot # 3240237Catalog# 324911Date of Event unknown Sample Status Discard. This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. (b)(6) 2026.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50912234 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC.Lot # 3240237.Catalog# 324911.Date of Event unknown. Sample Status Discard.This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available.(b)(6), 09 SEP 2026.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50911793 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC. Lot # 3240237.Catalog# 324911.Date of Event unknown.Sample Status Discard.This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. (b)(6) Perez 09 SEP 2026.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50911727 ↗MalfunctionSep 28, 2026Leak/Splash
Consumer Reported found 10 syringes when drawing insulin, the insulin leaked out the barrel / hub assembly. Discarded. - DC.Lot # 3240237.Catalog# 324911.Date of Event unknown.Sample Status Discard.This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken nine additional complaint record were created for defect leakage. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. (b)(6) 09 SEP 2026.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50911688 ↗MalfunctionSep 26, 2026Leak/Splash
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908051 ↗MalfunctionSep 26, 2026Leak/Splash
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908039 ↗MalfunctionSep 26, 2026Leak/Splash
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50908025 ↗MalfunctionSep 24, 2026Volume Accuracy Problem
Consumer reported, the first line on the barrel is different between 3 syringes. Stated, he did use the syringes.Lot: 3268200Catalog: 324910Date of Event: UnknownSamples: Yes CL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885599 ↗
Other Becton, Dickinson and Company Inc products
All Becton, Dickinson and Company Inc devices →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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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