Eclipse 303306Recalls & reported problems
Becton, Dickinson And Company · SYRINGE 3ML LL ECLIPSE 23X1-1/2 RB TW · Class 2
All models of Eclipse (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382903033065), received between Feb 6, 2025 and Feb 6, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Protrusion/Extrusion” (1 report).
1 other recall cover devices cleared under the same FDA submission (K161170); 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Protrusion/Extrusion1
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.
MalfunctionFeb 6, 2025Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT BD SYRINGE 3ML LL ECLIPSE 23X1-1/2 RB TW SAFETY SHIELD BROKE OFF IT WAS REPORTED BY CUSTOMER THAT THE GUARD OF THE INJECTION NEEDLE BROKEN WHEN IT WAS TO BE APPLIED AFTER THE INJECTION. RCC RECEIVED A COMPLAINT VIA EMAIL. PRODUCT CODE: 303306 PRODUCT DESCRIPTION: SYRINGE & NEEDLE 3CC 23G X 1.5IN L/L RB TW BX/50 LOT/SERIAL #: (B)(6) EXPIRY DATE: 2027-09-30. PROBLEM INFORMATION PRODUCT CONCERN TICKET NUMBER: (B)(4) (DATE OF INCIDENT: (B)(6)2024 CONCERN DESCRIPTION: THE GUARD ON AN INJECTION NEEDLE BROKE WHEN IT WAS TO BE APPLIED AFTER THE INJECTION. THIS DEVICE PROBLEM HAS OCCURED 4 TIMES OVER THE LAST YEAR WITH CLINICAN USER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21323664 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K161170. One submission often covers many models, so check the product and lot details in each record.
- Z-1440-2017 · Dec 20, 2016 · TerminatedEclipse Hypodermic Needle
Other Syringe, piston devices
- BD Luer-Lok 309657Becton, Dickinson And Company · Syringe, piston1,266 reports
- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
- BD Luer-Lok 309628Becton, Dickinson And Company · Syringe, piston862 reports
- N/A 302995Becton, Dickinson And Company · Syringe, piston1 recall537 reports
- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- N/A 302830Becton, Dickinson And Company · Syringe, piston462 reports
- N/A 302832Becton, Dickinson And Company · Syringe, piston424 reports
- BD Ultra-Fine 328468Becton, Dickinson and Company Inc · Syringe, piston323 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
- 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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