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WIEGAND

Asp Global, LLC · Model 202.95.11 · UDI-DI 00840216124486

OHY
0
510(k) clearances
38
Adverse events
1
Recalls
95
Facilities

Description

PILL CRUSHER POUCHES, WIEGAND, 50EA/BG, 20BG/BX, 8BX/CS (8000EA/CS)

Recalls

DateFirmReason
2022-05-11MEDLINE INDUSTRIES, LP - NorthfieldProduct lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.

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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.