Frigitronics 147Recalls & reported problems
Coopersurgical, Inc. · Micro, Curved Probe. Tip: 1.0mm diameter. Shaft: 27mm length x 1.0mm diameter. · 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 00888937004243), received between Sep 21, 2020 and Sep 21, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Temperature Problem” (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
- Temperature Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2020Temperature Problem
HAND PIECE GETS COLD. ORDER: 94625. THE HAND PIECE HANDLE WAS FREEZING TO THE SURGEONS GLOVES. ALSO THE HAND PIECE TIP WAS COLD TO TOUCH. REF E-COMPLAINT-(B)(4). 1 0MM CRVD MICRO W-TC 147 E-COMPLAINT-(B)(4).
Patient problems: Insufficient Information
MAUDE report 10560927 ↗
Other Unit, Cryotherapy, Ophthalmic devices
- Frigitronics 139Coopersurgical, Inc. · Unit, Cryotherapy, Ophthalmic3 reports
- Frigitronics 124Coopersurgical, Inc. · Unit, Cryotherapy, Ophthalmic2 reports
- Frigitronics CE-2000Coopersurgical, Inc. · Unit, Cryotherapy, Ophthalmic1 report
- Frigitronics 161Coopersurgical, Inc. · Unit, Cryotherapy, Ophthalmic1 report
- Frigitronincs 126Coopersurgical, Inc. · Unit, Cryotherapy, Ophthalmic1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.