Welch Allyn, Inc. 901027 (REF 77791-2MPXL)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn Green Series 777 Integrated Wall Diagnostic System with SureColor LED Technology including Wall Aneroid Sphygmomanometer (#7670-01), SureTemp Plus 690 Electronic Thermometer (#01690-300), PanOptic Ophthalmoscope with Cobalt-Blue Filter and Corneal Viewing Lens (#11820), MacroView Otoscope (#23810 · Class 2
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 21, 2025Class IIOpen, Classified
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Z-1566-2025 · Root cause: Device Design · Recall details · FDA record ↗
Other TRANSFORMER, ENDOSCOPE devices
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · TRANSFORMER, ENDOSCOPE1 recall0 reports
- Y/C cable MB-631Olympus Medical Systems Corp. · Transformer, Endoscope5 reports
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope2 reports
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · Transformer, endoscope2 reports
- Welch Allyn, Inc. 901027Welch Allyn, Inc. · Transformer, endoscope2 reports
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 report
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 report
- Welch Allyn, Inc. 901067Welch Allyn, Inc. · Transformer, endoscope1 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 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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