BD Nano 2nd GenRecalls & reported problems across all models
Becton Dickinson Pen Limited · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2,058
- Deaths reported
- 0
- Injuries reported
- 23
- Recalls
- 0
We found 2 models of BD Nano 2nd Gen by Becton Dickinson Pen Limited in the FDA's device registry (GUDID). Together they are named in 2,058 adverse event reports in the FDA's MAUDE database, received between Sep 12, 2019 and Sep 30, 2026 — classified as 23 injuries, 2,035 malfunctions.
The most frequently reported specific device problem is “Failure to Deliver” (1,341 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 Nano 2nd Gen problems
Device problems
- Failure to Deliver1,341
- Misconnection172
- Complete Blockage129
- Break122
- Leak/Splash109
- Defective Device103
- Failure to Prime48
- Defective Component39
Patient problems
- No Clinical Signs, Symptoms or Conditions1,777
- No Consequences Or Impact To Patient159
- No Known Impact Or Consequence To Patient51
- Pain36
- Hyperglycemia33
- Foreign Body In Patient17
- Bruise/Contusion8
- Skin Inflammation/ Irritation8
BD Nano 2nd Gen models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD Nano 2nd Gen 320550Needle, hypodermic, single lumen2,044 reports
- BD Nano 2nd Gen 320551Needle, hypodermic, single lumen14 reports
Recent BD Nano 2nd Gen adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954932 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954826 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954790 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954703 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954654 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954533 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954025 ↗MalfunctionSep 30, 2026Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953587 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950723 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950543 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950094 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949991 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949900 ↗MalfunctionSep 30, 2026Misconnection; Failure to Deliver
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949338 ↗MalfunctionSep 30, 2026Failure to Deliver
Consumer Reported found about 2 dozen pen needles from two different lot number. Unknown amount on each lot #. Needles would not prime. noticed after removed from pen the non patient end needle to be bent. DC Lot # 3017179 Lot # 3025239Catalog# unknown - 32g 4mm 2nd gen Date of Event Unknown Sample Status Awaiting sample
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50943940 ↗
Other Becton Dickinson Pen Limited products
All Becton Dickinson Pen Limited 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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