miLOOP 303071-9090-000Recalls & reported problems
Carl Zeiss Meditec AG · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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.
Recalls naming this device
- Mar 16, 2022Class IIOpen, Classified
High friction of the slider can cause the device to stick, or not move as intended.
Z-1007-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Hook, Ophthalmic devices
- Sklar Instruments 96-2224ASklar Corporation · Hook, ophthalmic1 recall0 reports
- Alcon Grieshaber 25+ Finesse 338.25PAlcon Laboratories, Inc. · Hook, ophthalmic21 reports
- Alcon Grieshaber 27+ Finesse 338.27Alcon Laboratories, Inc. · Hook, ophthalmic11 reports
- Alcon Grieshaber 337.92Alcon Laboratories, Inc. · Hook, ophthalmic2 reports
- Osher/Malyugin Ring Manipulator MAL-0003Microsurgical Technology, Inc. · Hook, Ophthalmic1 report
- Millennium 92-H0499Avalign Technologies, Inc. · Hook, ophthalmic1 report
- Alcon Greishaber Finesse 338.23Alcon Laboratories, Inc. · Hook, ophthalmic1 report
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
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- 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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