Tissue Retrieval System TRS175SB2Recalls & reported problems
Anchor Products Company · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00612376000012), received between Sep 18, 2018 and Sep 18, 2018 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Hemostasis1
- Tissue Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 18, 2018Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT THE TRS175SB2, TISSUE RETRIEVAL BAG'S WIRE POPPED OUT DURING BAG DEPLOYMENT AND DAMAGED THE CHEST WALL DURING A THORASCOPIC RIGHT INFERIOR LOBE RESECTION SURGERY. THE SURGEON USED THE ELECTRIC SCALPEL TO PROVIDE HEMOSTASIS TO THE CHEST WALL BLEEDING. THIS REPORT IS RAISED ON THE BASIS OF A REPORTED PATIENT INJURY.
Patient problems: Hemostasis; Tissue Damage
MAUDE report 7887070 ↗
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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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