BD Veo 324911Recalls & reported problems
Becton, Dickinson and Company Inc · BD Veo Insulin Syringes with BD Ultra-Fine Needle, U-100, 6mm, 31G, 0.5mL · Class 2
Quick summary
This BD Veo insulin syringe is a syringe with a fine needle used to inject insulin. Many of the 178 reports describe insulin leaking from the barrel, plungers that will not push and contamination inside the barrel. The reports include 175 malfunctions, 3 injuries and no deaths. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 189
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 189 adverse event reports that list this exact device (DI 00382903249114), received between Oct 24, 2017 and Sep 28, 2026 — classified as 3 injuries, 186 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (60 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
- Leak/Splash60
- Device Contamination with Chemical or Other Material24
- Failure to Deliver22
- Device Markings/Labelling Problem19
- Defective Device18
- Break10
- Volume Accuracy Problem10
- Material Separation9
Patient problems
- No Known Impact Or Consequence To Patient89
- No Clinical Signs, Symptoms or Conditions63
- No Consequences Or Impact To Patient29
- No Patient Involvement8
- Insufficient Information2
- Abrasion1
- Needle Stick/Puncture1
- No Information1
Recent adverse event reports
The 25 most recent of 189 reports, in the reporter's own words as published by the FDA.
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 18, 2026Device Markings/Labelling Problem
Patient problems: Insufficient Information
MAUDE report 50828517 ↗MalfunctionSep 18, 2026Device Markings/Labelling Problem
Patient problems: Insufficient Information
MAUDE report 50828465 ↗MalfunctionApr 17, 2025Failure to Deliver; Failure to Deliver
SPOUSE OF CONSUMER REPORTED THAT THE PLUNGER ROD WILL NOT DEPRESS WHEN DOING INJECTION. HE STATED THAT HE WAS ABLE TO DRAW THE INSULIN FROM THE VIAL. CONSUMER DOES NOT RE-USE. LOT#: 1350910, CATALOG#: 324911, DATE OF EVENT: UNKNOWN, SAMPLES: DISCARDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21857756 ↗MalfunctionApr 17, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
SPOUSE OF CONSUMER REPORTED THERE IS "CLEAR LIQUID" COMING FROM THE BARREL ONTO THE NEEDLE BEFORE USE AND WANTED TO KNOW IF SAFE TO TAKE INJECTION. LOT: 4225140, CATALOG: 324911, DATE OF EVENT: UNKNOWN, SAMPLES: YES CL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21857594 ↗MalfunctionJun 13, 2024Leak/Splash; Leak/Splash
CONSUMER LEFT VOICEMAIL REPORTING THAT THE RUBBER STOPPER SEPARATED FROM THE PLUNGER ROD. CONSUMER PROVIDED MAILING ADDRESS AND REQUESTED A MAIL KIT TO RETURN SAMPLES. I RETURNED CONSUMER'S CALL AND LEFT VOICEMAIL FOR RETURN CALL. LOT #: UNKNOWN. CATALOG #: UNKNOWN. DATE OF EVENT: UNKNOWN. SAMPLES: AVAILABLE - SENDING MAIL KIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19533256 ↗MalfunctionJun 10, 2024Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
REPRESENTATIVE FROM A MAIL ORDER PHARMACY CALLED TO REPORT AN ISSUE ON THE CONSUMERS BEHALF. STATED, CONSUMER IS SEEING "BLACK STREAKS" INSIDE THE BARREL PRIOR TO INJECTION. STATED, SHE CANNOT SEE THE "BLACK STEAKS" UNTIL SHE DRAWS UP THE INSULIN. STATED, WHEN THE CONSUMER DRAWS UP HER INSULIN, SHE CANNOT SEE IF "AIR BUBBLES" ARE THERE. STATED, THE CONSUMER IS STILL TAKING HER INJECTION WITH THE SYRINGES THAT HAVE "BLACK STREAKS". STATED, THE PHARMACY WILL BE REPLACING TWO BOXES FOR THE CONSUMER LOT: 4009038. CATALOG: 324911. DATE OF EVENT: UNKNOWN. SAMPLES: YES CL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19505569 ↗MalfunctionMay 16, 2024Leak/Splash; Leak/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.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19336628 ↗MalfunctionSep 20, 2023Material Separation; Material Separation
IT WAS REPORTED THAT THE NEEDLE HUB SEPARATED WITH THE BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE. THE FOLLOWING WAS RECEIVED BY THE INITIAL REPORTER: CONSUMER REPORTED FOUND 1 SYRINGE REMOVED NEEDLE SHIELD AND HUB ASSEMBLY WAS STUCK IN SHIELD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17785425 ↗MalfunctionJun 26, 2023Failure to Deliver; Failure to Deliver
IT WAS REPORTED WHILE USING BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE IT WAS DIFFICULT TO ASPIRATE THE SYRINGE. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED THAT THE SYRINGES WILL NOT DRAW. LOT #: 1347677 CATALOG #: 324911 DATE OF EVENT: UNKNOWN SAMPLES: AVAILABLE - SENDING MAIL KIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17199045 ↗MalfunctionJun 15, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT PRIOR TO USE WITH BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE THE SCALE MARKINGS WERE MISSING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "1 DEFECTIVE SYRINGE IN PACKAGE OF 10 SYRINGE MISSING VOLUME LABELS, NEEDED TO USE 3 UNITS BUT THERE WAS NONE SO SHE COULDN'T USE IT".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17140098 ↗MalfunctionFeb 26, 2023Component Missing; Defective Device; Component Missing; Defective Device
IT WAS REPORTED THAT THE BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE WAS DAMAGED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: SYRINGE PLUNGER DEFORMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16441326 ↗MalfunctionFeb 10, 2023Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED WHILE USING BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE 1/2ML 6MM THERE WAS A SHARP PROTRUSION ON THE PLUNGER. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED THAT THERE IS A SHARP EDGE UNDER THE THUMB PRESS ON THE PLUNGER ROD. HE STATED THAT HE GETS CUT WHEN HE PULLS THE PLUNGER ROD OUT, STATED THAT THE CUT IS SIMILAR TO A PAPER CUT.
Patient problems: Abrasion
MAUDE report 16358497 ↗MalfunctionDec 22, 2022Material Separation; Material Separation
IT WAS REPORTED THAT THE BD VEO¿ INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE HUB SEPARATED FROM THE SYRINGE DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CONSUMER REPORTED NEEDLE HUB SEPARATED AND STAYED IN THE SHIELD."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16040510 ↗MalfunctionSep 29, 2022Material Separation; Material Separation
IT WAS REPORTED THAT 50 BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE CAME OFF THE SYRINGE WITH SHIELD. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WHEN REMOVING THE NEEDLE SHIELDS, THE NEEDLE ASSEMBLY CAME OFF SYRINGE WITH SHIELD
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15505964 ↗MalfunctionSep 8, 2022Failure to Deliver; Physical Resistance/Sticking; Failure to Deliver; Physical Resistance/Sticking
IT WAS REPORTED THAT THE BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ GETS STUCK IN BARREL. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: STATED, STOPPER GETS STUCK IN BARREL MAKING IT HARD TO DRAW UP INSULIN BECAUSE PLUNGER ROD GETS STUCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15375990 ↗MalfunctionSep 8, 2022Material Separation; Material Separation
IT WAS REPORTED THAT THE BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLE HUB SEPARATES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: RECEIVED VOICEMAIL FROM CONSUMER STATING, WHEN HE REMOVES NEEDLE SHIELD, NEEDLE HUB SEPARATES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15375946 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.