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Safety 1st

DOREL JUVENILE GROUP, INC. · Model IH601 · UDI-DI 00884392954451

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10
510(k) clearances
25
Adverse events
1
Recalls
234
Facilities

Description

ESSENTIAL SICK-DAY SCREENING KIT

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

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

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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.