Home › WELCH ALLYN, INC. › Welch Allyn, Inc.

Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901026 · UDI-DI 00732094016345

ERA Prescription

510(k) clearances

Adverse events

Recalls

234

Facilities

Description

Welch Allyn 3.5 V Halogen HPX Ophthalmic Set including PanOptic Ophthalmoscope with Cobalt-Blue Filter on Corneal Viewing Lens (#11820), Prestige Coaxial-Plus Ophthalmoscope (#11735), Elite Streak Retinoscope (#18245), Fiber-Optic Finnoff Ocular Transilluminator (#41100), One Rechargeable 120-Minute Power Handle and One Rechargeable 60-Minute Power Handle

Recalls

Date	Firm	Reason
2025-05-09	Baxter Healthcare Corporation	The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to ex

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.