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ASP MEDICAL

Asp Global, LLC · Model PP993 · UDI-DI 00840216104303

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

Description

PILLCRUSHERPOUCH, 1/EA,8000/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.