ACCEL® 622299Recalls & reported problems
B Braun Interventional Systems, Inc · 600ML DRAI.BOTTLE,DR600LOCK,PVC-FREE,FPS · Class 2 · Implant
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 04046955323494), received between Feb 16, 2023 and May 5, 2023 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Suction Problem” (10 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.
Most reported problems
Device problems
- Suction Problem10
Patient problems
- No Clinical Signs, Symptoms or Conditions10
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 5, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 1: DETAILED INQUIRY DESCRIPTION: AFTER CONNECTING THE ACCEL BOTTLES THE NURSES REALIZED THAT THE VACUUM HAD BEEN LOST SO NO SUCTION OCCURRED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16875371 ↗MalfunctionMay 5, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 2: DETAILED INQUIRY DESCRIPTION: AFTER CONNECTING THE ACCEL BOTTLES THE NURSES REALIZED THAT THE VACUUM HAD BEEN LOST SO NO SUCTION OCCURRED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16875370 ↗MalfunctionMay 5, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 3: DETAILED INQUIRY DESCRIPTION: AFTER CONNECTING THE ACCEL BOTTLES THE NURSES REALIZED THAT THE VACUUM HAD BEEN LOST SO NO SUCTION OCCURRED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16875369 ↗MalfunctionMay 5, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 4: DETAILED INQUIRY DESCRIPTION: AFTER CONNECTING THE ACCEL BOTTLES THE NURSES REALIZED THAT THE VACUUM HAD BEEN LOST SO NO SUCTION OCCURRED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16875368 ↗MalfunctionApr 26, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 1: DETAILED INQUIRY DESCRIPTION: THE BOTTLES DON'T HAVE VACUUM. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16814465 ↗MalfunctionApr 26, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 2: DETAILED INQUIRY DESCRIPTION: THE BOTTLES DON'T HAVE VACUUM. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16814441 ↗MalfunctionApr 26, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 3: DETAILED INQUIRY DESCRIPTION: THE BOTTLES DON'T HAVE VACUUM. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16814440 ↗MalfunctionFeb 16, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 3: EVENT DESCRIPTION: THE SUCTION WOULD NOT ENGAGE WHEN THE WHITE CLAMP WAS DISLODGED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16385329 ↗MalfunctionFeb 16, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 2: EVENT DESCRIPTION: THE SUCTION WOULD NOT ENGAGE WHEN THE WHITE CLAMP WAS DISLODGED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16385328 ↗MalfunctionFeb 16, 2023Suction Problem; Suction Problem
AS REPORTED BY THE USER FACILITY: EVENT 1: EVENT DESCRIPTION: THE SUCTION WOULD NOT ENGAGE WHEN THE WHITE CLAMP WAS DISLODGED. NO INJURY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16385327 ↗
Other BOTTLE, COLLECTION, VACUUM devices
- OASIS 3600-100Atrium Medical Corporation · Bottle, Collection, Vacuum3 recalls1 death175 reports
- OCEAN 2002-000Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM3 recalls44 reports
- EXPRESS 16400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall110 reports
- EXPRESS 4000-100NAtrium Medical Corporation · Bottle, Collection, Vacuum2 recalls30 reports
- OCEAN 2002-400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM2 recalls18 reports
- OASIS 3612-100Atrium Medical Corporation · Bottle, Collection, Vacuum1 recall18 reports
- Medline DYNDSCL1500Medline Industries, Inc. · BOTTLE, COLLECTION, VACUUM1 recall13 reports
- PNEUMOSTAT 16100Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall3 deaths12 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.