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WELLSTAR

Asp Global, LLC · Model WSGNA450L2 · UDI-DI 00840216125902

OEA
0
510(k) clearances
42
Adverse events
17
Recalls
559
Facilities

Description

GOWN, WELLSTAR ISOLATION AAMI LEVEL 2, YELLOW W/WELLSTAR LOGO IN BLACK INK ON LEFT CHEST, UNIVERSAL, OVER THE HEAD, FULL BACK, TIE WAIST, THUMBHOOK W/ELASTIC WRIST, 10EA/BG, 10BG/CS, (100EA/CS)

Recalls

DateFirmReason
2024-06-03Stryker CorporationExpired Products distributed to customers
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.
2021-01-07Cardinal Health 200, LLCThere is a potential for rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns and lab coats.

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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.