FDA daily for Thursday, February 8, 2024
In this issue: 16 approvals, 24 device recalls, 13 device decisions and 93 label changes. 5 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.
- AZMIRO
AZURITY · TESTOSTERONE CYPIONATE
- smiths medical Medfusion Model 3500 Syringe pump
Smiths Medical ASD Inc. · Medfusion syringe pumps, with software versions before v6.0.0, may have the following issues:1. Delivery During Motor Not Running High Priority Alarm, 2. Infus…
- smiths medical Medfusion Model 4000 syringe pump
Smiths Medical ASD Inc. · Medfusion Model 4000 syringe infusion pumps, with the following software versions, may have the following issues: 1. Delivery During Motor Not Running High Pri…
- EltaMD UV Lip Balm SPF31
ZINC OXIDE AND OCTINOXATE SUNSCREEN · CP Skin Health, Inc · TOPICAL
Drug and biologic approvals
FDA date:On Thu, Feb 1 FDA approved 2 new applications (0 brand or biologic, 2 generic) and 14 supplements to existing ones.
- METHSCOPOLAMINE BROMIDE
NE RX PHARMA · METHSCOPOLAMINE BROMIDE
- BUTALBITAL AND ACETAMINOPHEN
QUAGEN · ACETAMINOPHEN, BUTALBITAL
- AZMIRO
AZURITY · TESTOSTERONE CYPIONATE
Device recalls
FDA date:FDA posted 24 device recalls from 6 firms on Thu, Feb 1.
- smiths medical Medfusion Model 3500 Syringe pump
Smiths Medical ASD Inc. · Medfusion syringe pumps, with software versions before v6.0.0, may have the following issues:1. Delivery During Motor Not Running High Priority Alarm, 2. Infus…
- smiths medical Medfusion Model 4000 syringe pump
Smiths Medical ASD Inc. · Medfusion Model 4000 syringe infusion pumps, with the following software versions, may have the following issues: 1. Delivery During Motor Not Running High Pri…
- Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Achieva 1.5T Conversion. Model (REF) Numbers 781346, 781283.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Achieva 1.5T Initial system. Model (REF) Numbers 781178.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Achieva 3.0T. Model. (REF) Numbers 781277, 781177, 781278, 781344, 781345.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Achieva XR. Model (REF) Numbers 781153, 781253.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Ingenia 1.5T CX. Model (REF) Numbers 781262, 781261.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Intera 1.5T Achieva Nova-Dual. Model (REF) Number 781173.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
- Intera Achieva 1.5T Pulsar. Model (REF) Number 781171.
Philips North America · The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the sc…
Device clearances and approvals
FDA date:FDA decided 8 510(k)s and 5 PMA decisions on Thu, Jan 25.
- AlphaVent Knotless SP PEEK Anchor
Stryker Endoscopy · Orthopedic
- ADIRA Lateral Plate System
Globus Medical, Inc. · Orthopedic
- FlexTip Bipolar electrodes single-use (AR-S9805-0028), FlexTip Bipolar electrodes single-use (AR-S9805-0035)
Sutter Medizintechnik GmbH · General, Plastic Surgery
- GentleCath Air for Women (CH10); GentleCath Air for Women (CH12); GentleCath Air for Women (CH14)
Convatec · Gastroenterology, Urology
- MR Q; MR Q SUPINE; MR Q SLT
Meridian AG · Ophthalmic
- BreView
GE Medical Systems SCS · Radiology
- Clariti 1 day Multifocal (somofilcon A) Soft (Hydrophilic), Daily Disposable Contact Lens with UV Blocker
CooperVision, Inc. · Ophthalmic
- Facet Aurora Reusable Lancet Base
Facet Technologies, LLC · General, Plastic Surgery
Label updates
FDA date:93 drug labels took effect on Thu, Jan 25; 4 of the 25 read for this issue are for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.
- EltaMD UV Lip Balm SPF31
ZINC OXIDE AND OCTINOXATE SUNSCREEN · CP Skin Health, Inc · TOPICAL
- Droxidopa
DROXIDOPA · MAJOR PHARMACEUTICALS · ORAL
- COCAINE HYDROCHLORIDE
COCAINE HYDROCHLORIDE · LXO US INC. · NASAL
- Ziprasidone Hydrochloride
ZIPRASIDONE HYDROCHLORIDE · NuCare Pharmaceuticals,Inc. · ORAL
- Corvert
IBUTILIDE FUMARATE · Pharmacia & Upjohn Company LLC · INTRAVENOUS
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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