Welch Allyn, Inc. 901122 (REF 106364)Recalls & reported problems
Welch Allyn, Inc. · SPOT VS POWER SUPPLY SET PLUG2 EUR · Class 1
Data updated Oct 18, 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 18, 2026.
Recalls naming this device
- Mar 26, 2024Class IIOpen, Classified
Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.
Z-1510-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other Refractometer, ophthalmic devices
- Welch Allyn, Inc. 901029Welch Allyn, Inc. · Refractometer, ophthalmic1 recall11 reports
- Welch Allyn, Inc. 901122Welch Allyn, Inc. · Refractometer, ophthalmic1 recall0 reports
- Welch Allyn, Inc. 901029Welch Allyn, Inc. · Refractometer, ophthalmic18 reports
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 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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