FDA daily for Tuesday, June 11, 2024
In this issue: 18 approvals, 75 device recalls, 11 device decisions and 129 label changes. 4 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.
- VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the…
Ortho-Clinical Diagnostics, Inc. · The results generated by the VITROS Immunodiagnostic Products Vitamin B12 Range Verifier Lot# 1200 RV Level 2 may cause range verification failure. The issue i…
- Nitrile Disposable Examination Gloves, Tested for Use with Chemotherapy Drugs and Fentanyl
Xingyu Medical Tech Co., Ltd. · General Hospital
Drug and biologic approvals
FDA date:On Tue, Jun 4 FDA approved 4 new applications (1 brand or biologic, 3 generic) and 14 supplements to existing ones.
- CARBIDOPA AND LEVODOPA
RUBICON RESEARCH · CARBIDOPA, LEVODOPA
- TERIPARATIDE
ALMAJECT · TERIPARATIDE
- ALENDRONATE SODIUM
IPCA LABS LTD · ALENDRONATE SODIUM
- LOSARTAN POTASSIUM
APOTEX · LOSARTAN POTASSIUM
Device recalls
FDA date:FDA posted 75 device recalls from 5 firms on Tue, Jun 4.
- VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the…
Ortho-Clinical Diagnostics, Inc. · The results generated by the VITROS Immunodiagnostic Products Vitamin B12 Range Verifier Lot# 1200 RV Level 2 may cause range verification failure. The issue i…
- Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.
LEICA BIOSYSTEMS NUSSLOCH GMBH · Poorly processed and/or damaged biopsy tissue specimens on the device resulting from reagent levels exceeding the maximum fill level marks on reagent bottles o…
- HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064…
Philips North America Llc · Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
- HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064…
Philips North America Llc · Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
- HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100…
Philips North America Llc · Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
- ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 6X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
Atrium Medical Corporation · Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
Device clearances and approvals
FDA date:FDA decided 10 510(k)s and 1 PMA decision on Tue, May 28.
- Nitrile Disposable Examination Gloves, Tested for Use with Chemotherapy Drugs and Fentanyl
Xingyu Medical Tech Co., Ltd. · General Hospital
- EVOLVE Nitric Oxide Delivery System
Malinckrodt Manufacturing, LLC · Anesthesiology
- Regenalase Laser System
Ipg Medical · General, Plastic Surgery
- Luna Diode Laser System (TL-S20S-TWC, TL-S20S-755A , TL-S20S-810B)
Theralaser Medtech (China) Co., Ltd. · General, Plastic Surgery
- SpiroSphere, SpiroSphereECG, CardioSphere
Eresearchtechnology GmbH · Anesthesiology
- Laser Speckle Imaging System (RFLSI CZW)
Rwd Life Science Co., Ltd. · Cardiovascular
- Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5)
Enpuno Biotechnology Co., Ltd. · Dental
- React 71 Catheter
Micro Therapeutics Lnc. D/B/A Ev3 Neurovascular · Cardiovascular
- PILLAR SA Ti Spacer System (82-XXX)
Orthofix, Inc. · Orthopedic
- ANNE Limb
Sibel Health, Inc. · Cardiovascular
Label updates
FDA date:129 drug labels took effect on Tue, May 28; 3 of the 25 read for this issue are for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.
- Nadolol
NADOLOL · BluePoint Laboratories · 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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