FDA daily for Friday, May 24, 2024
In this issue: 15 approvals, 35 device recalls, 24 device decisions and 49 label changes. 6 items touch categories MedGrid carries, and they come first.
For MedGrid's categories
Items in this issue that name a product category sold on MedGrid. Each links to its full FDA record; the chip opens that category's federal and state rules.
- MUSE
VIATRIS · ALPROSTADIL
- Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Num…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Disposable infusion set with needle
Shandong Zhushi Pharmaceutical Group Co., Ltd. · General Hospital
- Filter Needle for Single Use
Hangzhou Qiantang Longyue Biotechnology Co., Ltd. · General Hospital
Drug and biologic approvals
FDA date:On Fri, May 17 FDA approved 4 new applications (0 brand or biologic, 4 generic) and 11 supplements to existing ones.
- EMTRICITABINE AND TENOFOVIR ALAFENAMIDE FUMARATE
APOTEX · EMTRICITABINE, TENOFOVIR ALAFENAMIDE FUMARATE
- DEFERASIROX
PHARMOBEDIENT · DEFERASIROX
- PREGABALIN
REGCON HOLDINGS · PREGABALIN
- ARFORMOTEROL TARTRATE
NEOCUBES PHARMA · ARFORMOTEROL TARTRATE
- MUSE
VIATRIS · ALPROSTADIL
Device recalls
FDA date:FDA posted 35 device recalls from 2 firms on Fri, May 17.
- Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Num…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): (…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 1.5T Conversion- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Numb…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 1.5T Initial system Model Number (REF): 781178
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 3.0T Model Number (REF): (1) 781345; (2) 781344; (3) 781278; (4) 781277; (5) 781177
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Achieva 3.0T TX for PET Model Number (REF): 781479
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- AchievaXR -Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Number (REF): 7812…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Evolution upgrade 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device Model Numbe…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Evolution upgrade 3.0T Model Number (REF): (1)782117; (2) 782143
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Ingenia 1.5T Model Number (REF): (1) 782140; (2) 782115; (3) 782101; (4) 781396; (5) 781341; (6) 781315
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
- Ingenia 1.5T CX - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (RE…
Philips North America Llc · The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's tech…
Device clearances and approvals
FDA date:FDA decided 16 510(k)s and 8 PMA decisions on Fri, May 10.
- Disposable infusion set with needle
Shandong Zhushi Pharmaceutical Group Co., Ltd. · General Hospital
- Filter Needle for Single Use
Hangzhou Qiantang Longyue Biotechnology Co., Ltd. · General Hospital
- Bioceramic Root Repair Material (C-Root BP)
Beijing C-Root Dental Medical Devices Co., Ltd. · Dental
- Access OV Monitor
Beckman Coulter, Inc. · Immunology
- HyperSuture Extension Line
Threadstone, LLC · General, Plastic Surgery
- Ureterorenoscope System
Shenzhen HugeMed Medical Technical Development Co., Ltd. · Gastroenterology, Urology
- Dochek® Multi-Drug Urine Test Dipcard Rx; Dochek® Multi-Drug Urine Test Dipcard
Guangzhou Decheng Biotechnology Co., Ltd. · Clinical Toxicology
- SCARLET® AC-Ti
Spineart SA · Orthopedic
- Aerogen®Solo Nebulizer System
Aerogen, Ltd. · Anesthesiology
- pureFLOW 402 (F00012067); pureFLOW 406 (F00012068); pureFLOW 401 (F00012069); pureFLOW 400 (F00012070)
Fresenius Medical Care Renal Therapies Group, LLC · Gastroenterology, Urology
- Oocyte Flushing & Retrieval Medium; Gamete Buffer
Gimbo Medical Technology Shenzhen Co., Ltd. · Obstetrics/Gynecology
- SmartChest
Milvue · Radiology
- QIAstat-Dx® Respiratory Panel Plus
QIAGEN GmbH · Microbiology
- APERTO Lucent MRI System
FUJIFILM Healthcare Americas Corporation · Radiology
- PillCam Genius SB System with PillCam Software v9.7 and PillCam Cloud Reader Software
Given Imaging Ltd. (D.B.A. Medtronic) · Gastroenterology, Urology
Label updates
FDA date:49 drug labels took effect on Fri, May 10; 4 of the 25 read for this issue are for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.
- Jack Black
TITANIUM DIOXIDE, ZINC OXIDE · Jack Black L.L.C · TOPICAL
- Protectif Fair Tint
ZINC OXIDE AND TITANIUM DIOXIDE · Allure Labs · TOPICAL
- Clobazam
CLOBAZAM · Chartwell RX, LLC · ORAL
How the FDA daily is written
Every issue is written from FDA's public data (openFDA) and nothing else: the counts, names, firms and reasons are FDA's own. openFDA posts each kind of record on its own delay, so each section covers one FDA date and says which. Shortages cover yesterday; approvals, drug and device recalls, and food and supplement recalls cover a week ago; device clearances and label changes cover two weeks ago. Every FDA date appears in exactly one issue. Complete response letters appear the day after FDA publishes a batch.
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