FDA Device Intelligence
HomeDynarex Corporation › Blood Collection Tube Holders

Blood Collection Tube Holders

Dynarex Corporation · Model 6934 · UDI-DI 00616784693422

KST
0
510(k) clearances
71
Adverse events
4
Recalls
81
Facilities

Description

Blood Collection Tube Holders with Luer Lock

Recalls

DateFirmReason
2015-10-01Hummingbird MedHummingbird Med Devices, Inc. is recalling ABG-HM-1 Hummi Micro Draw Blood Transfer because the connection between the "Hummi" Y connector and the yellow cannula hub may not be suf
2015-03-11Hummingbird MedHummingbird Med Devices, Inc. is recalling the Hummi Micro Draw because of insertion difficulties.
2013-02-06Heritage Labs International LLCThe product has a Lithium Heparin contaminant which could adversely affect coagulation results potentially causing erroneous lab results.
2011-04-22Becton Dickinson & CompanyBD Vacutainer Push Button Blood Collection Set can potentially undergo cannula separation from the hub.

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 keyRead 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.