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🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Submission for Office of Management and Budget Review; Office of Refugee Resettlement Unaccompanied Refugee Minors Program Application and Withdrawal of Unaccompanied Refugee Minors Program Application or Declination of Unaccompanied Refugee Minors Program Placement Forms
The Office of Refugee Resettlement is requesting a 3-year extension with revisions of the Unaccompan...
Federal RegisterOriginal source
🇺🇸Regulatoryfederalregister.govTier 1 · Regulatory source
Request for Information (RFI): Inviting Comments and Suggestions on Topic Areas for the NIDCR Strategic Plan for Fiscal Years 2027-2031
The National Institute of Dental and Craniofacial Research (NIDCR) is developing its Strategic Plan...
Federal RegisterOriginal source
🇹🇭Regulatoryfda.moph.go.thTier 1 · Regulatory source
15 ก.ค. 69ข่าวประกาศผลการตรวจพิสูจน์อาหาร อย. แจ้งเตือนประชาชน หยุดบริโภคผลิตภัณฑ์อาหาร 25 รายการ หลังตรวจพบเป็นอาหารปลอมอ่านเพิ่มเติม →
สำนักงานคณะกรรมการอาหารและยา ได้ประสานสำนักงานสาธารณสุขจังหวัดศรีสะเกษ ดำเนินการตรวจสอบสถานที่ผลิตอา...
Thai FDAOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Drug recall: Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01
Official structured record identifier: 99312.
openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Drug recall: Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.
Official structured record identifier: 99311.
openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Drug recall: Clomiphene Citrate USP Active Pharmaceutical Ingredient (CAS : 50-41-9), Net Weight a)1 KG (NDC 84849-000-01), b) 500 g (NDC 84849-000-02), (c) 100 g (NDC 84849-000-03), Rx Only, Shimoga Chemicals Address -W-57A, MIDC Kupwad Samgli, Maharashtra, 416436, India.
Official structured record identifier: 99232.
openFDA Drug RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed
Official structured record identifier: 99280.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by pr
Official structured record identifier: 99219.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/
Official structured record identifier: 99106.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
Official structured record identifier: 99065.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: 5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing S
Official structured record identifier: 99061.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACE
Official structured record identifier: 98933.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
Official structured record identifier: 98704.
openFDA Device RecallsOriginal source
🇺🇸Regulatoryopen.fda.govTier 1 · Regulatory source
Device recall: Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Official structured record identifier: 98700.
openFDA Device RecallsOriginal source