FDA Device Intelligence
Home › WELCH ALLYN, INC. › Welch Allyn, Inc.

Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901082 · UDI-DI 00732094088717

ERA Prescription
10
510(k) clearances
23
Adverse events
1
Recalls
234
Facilities

Description

Welch Allyn PocketScope 2.5 V Halogen Ophthalmoscope with AA-Battery Handle, Soft Storage Case; 2 Alkaline AA Batteries

Recalls

DateFirmReason
2025-05-09Baxter Healthcare CorporationThe 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 keyRead 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.