NA 891400045Recalls & reported problems
Richard Wolf GmbH · SUCTION PUNCH Ø 4.5MM with integrated suction channel, WL 110 mm, take-apart, reusable · Class 1
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 04055207006993), received between Sep 16, 2019 and Sep 16, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2019Break; Break
ON AUGUST 13, 2019, RICHARD WOLF GMBH (RW GMBH) RECEIVED THE FOLLOWING INFORMATION: DURING AN ARTHROSCOPY OF A KNEE JOINT, A PINHEAD-SIZED PIECE OF THE TIP OF THE PUNCH REMAINED IN THE PATIENT'S JOINT AFTER THE INSERTION OF THE SUCTION BITE PUNCH AND WAS WASHED INTO THE POSTERIOR PARTS OF THE KNEE JOINT BY THE IRRIGATION PRESSURE.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 9072969 ↗
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- NA 251723Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC145 reports
- COBRA 3910900093Stryker Corporation · Accessories, arthroscopic138 reports
- FirstPass 72290129Smith & Nephew, Inc. · Accessories, arthroscopic82 reports
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- MITEK 242025Medos International Sàrl · ACCESSORIES,ARTHROSCOPIC61 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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