BD BBL™ DrySlide™ PYR Kit 231747Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ DrySlide™ PYR Kit · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382902317470), received between Aug 13, 2018 and Aug 13, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (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
- Tear, Rip or Hole in Device Packaging1
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 13, 2018Tear, Rip or Hole in Device Packaging
IT WAS REPORTED THAT WHILE USING A BD BBL¿ DRYSLIDE¿ PYR KIT A TECHNICIAN RECEIVED A CUT FROM A GLASS AMPOULE THAT WENT THROUGH THE PACKAGING. THE PATIENT RECEIVED MEDICAL EVALUATION FOLLOWING THE INCIDENT AND WAS MONITORED FOR FEVER AND INFECTION.
Patient problems: Laceration(s)
MAUDE report 7777327 ↗
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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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