SiluetaYa is recalling its tejocote root because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides, which are highly toxic to humans and animals. Ingestion of yellow oleand
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FDA-TRACK: Prescription Drug User Fee Act Meeting Goals SummaryWedgewood Connect, LLC. San Jose, CA. 483 issued 07/03/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 07/03/2025
Short Title (70 char) Wedgewood Connect, LLC. San Jose, CA. 483 issued 07/03/2025
FEI Number 3003434972
Firm Name Wedgewood Connect, LLC
Record Type 483
State CA
Establishment Type Outsourcing FacilitDr. Reddy’s Laboratories, Mirfield, West Yorkshire, UK 9.1-9.5.25_483
Record Date: 09/05/2025
Entity Name: Dr. Reddy’s Laboratories (EU) Ltd.
FEI Number: 3002807544
Record Type: 483
Country: United Kingdom
Establishment Type: API ManufacturerBlendHouse Allerton LLC. Allerton, IA. EIR issued 02/20/2025
Task Description Request Please post to the OII FOIA Electronic Reading Room
Record Date 02/20/2025
Short Title (70 char) BlendHouse Allerton LLC. Allerton, IA. EIR issued 02/20/2025
FEI Number 1921383
Firm Name BlendHouse Allerton LLC
Record Type EIR
State IA
Establishment Type ManufacturerUpdate on Alert: Infusion Set Performance Issue from BD
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program.
