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ACS CDLS14ERecalls & reported problems

American Contract Systems, Inc. · CMC LAPAROSCOPY · Class 2

Data updated Oct 13, 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 00191072046192), received between Nov 15, 2019 and Nov 15, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 15, 2019Device Contamination with Chemical or Other Material

    HAIR FOUND ON BLUE DISPOSABLE TOWEL IN LAPAROSCOPY PACK. DISPOSABLE TOWEL FROM PACK WAS OPENED/UNFOLDED TO PASS TO SURGEON FOR DRAPING AND A HAIR (BLACK, APPROX 1 INCH LONG) WAS DISCOVERED; DISPOSABLE TOWEL WITH CONTAMINANT AND OTHER DISPOSABLE TOWELS REMOVED FROM FIELD; SCRUB CHANGED GLOVES.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9327670 ↗

Other General surgery tray devices

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Sources and updates

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