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NA 110037Recalls & reported problems

Smith & Nephew, Inc. · FEMORAL CANAL SUCTION ABSORBER STANDARD 19MM DIAMETER · Class 2

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 03596010033321), received between Nov 4, 2022 and Nov 4, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • InjuryNov 4, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED THAT, DURING THR, AFTER WASHING THE FEMUR, THE SPONGE PART OF A FEM CANAL SUC ABSORB STD REMAINED IN THE BONE. THE SPONGE WAS REMOVED. THE PROCEDURE WAS COMPLETED, WITHOUT DELAY, WITH THE SAME DEVICE. PATIENT WAS NOT HARMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15726930 ↗

Other CATHETER AND TIP, SUCTION devices

All CATHETER AND TIP, SUCTION devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.