Home › Dynarex Corporation › Lab Coat Knitted Cuffs & Collar Without Pockets, X-Large, Blue

Lab Coat Knitted Cuffs & Collar Without Pockets, X-Large, Blue

Dynarex Corporation · Model 1995 · UDI-DI 00616784199528

LYU OEA

510(k) clearances

127

Adverse events

Recalls

803

Facilities

Recalls

Date	Firm	Reason
2023-05-18	MEDLINE INDUSTRIES, LP - Northfield	Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
2023-05-15	MEDLINE INDUSTRIES, LP - Northfield	Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2021-01-07	Cardinal Health 200, LLC	Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
2017-09-11	Zimmer Biomet, Inc.	Cut resistant surgical glove liners lack sterility assurance.

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 key Read 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.