BD Sharps Collector 305622Recalls & reported problems
Becton, Dickinson And Company · SHARPS COLL 3GAL PHARM · Class 2
All models of BD Sharps Collector (34)
Data updated Oct 18, 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 00382903056224), received between Jul 8, 2022 and Jul 8, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Missing” (1 report).
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 18, 2026.
Most reported problems
Device problems
- Component Missing1
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.
MalfunctionJul 8, 2022Component Missing; Component Missing
IT WAS REPORTED WHILE USING BD¿ PHARMACEUTICAL WASTE COLLECTOR THE ABSORBING PAD WAS MISSING. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED BY THE DISTRIBUTOR THAT ABSORBENT PAD WAS NOT INCLUDED WITH SHARPS COLLECTOR. VERBATIM: DISTRIBUTOR: HER CUSTOMER STATES THIS PAD WAS NOT INCLUDED WITH THE SHARPS COLLECTOR THEY RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14957562 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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