SPOTLIGHT 292908111Recalls & reported problems
Depuy Spine, LLC · SPOTLIGHT ACCESS SYSTEM 11F SUCTION TUBE RETRACTOR ASSEMBLY · Class 2
- 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 10705034225920), received between Sep 23, 2024 and Sep 23, 2024 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionSep 23, 2024Break; Break
IT WAS REPORTED THAT ON (B)(6) 2024 THE TIP OF THE SUCTION DEVICE BROKE WHEN WAS BEING USED. THE TIP GOT STUCK ON THE BONE BUT IT WAS POSSIBLE TO TAKE IT OUT. THERE WAS NO SURGICAL DELAY. THE PROCEDURE WAS SUCCESSFULLY COMPLETED. THERE WERE NO PATIENT CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20280494 ↗
Other CATHETER AND TIP, SUCTION devices
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- Wayne G56537Cook Incorporated · CATHETER AND TIP, SUCTION2 recalls33 reports
- Bard® Suction Connector EN0066000C. R. Bard, Inc. · CATHETER AND TIP, SUCTION1 recall6 reports
- Argyle 10142Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 12191Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Medline Industries, Inc. OR929KMedline Industries, Inc. · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 12102Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
- Argyle 10102Cardinal Health 200, LLC · CATHETER AND TIP, SUCTION1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.