FDA daily for Monday, August 10, 2026
In this issue: 12 approvals, 15 device recalls, 15 device decisions and 154 label changes. 3 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.
- Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Medical Action Industries, Inc. 306 · Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
- ND Needle Guidance System
Accurate Access, LLC · Radiology
- Liraglutide
LIRAGLUTIDE · Meitheal Pharmaceuticals Inc. · SUBCUTANEOUS
Drug and biologic approvals
FDA date:On Mon, Aug 3 FDA approved 2 new applications (0 brand or biologic, 2 generic) and 10 supplements to existing ones.
- NINTEDANIB ESYLATE
MACLEODS PHARMS · NINTEDANIB ESYLATE
- INDOCYANINE GREEN
ZYDUS LIFESCIENCES · INDOCYANINE GREEN
Device recalls
FDA date:FDA posted 15 device recalls from 7 firms on Mon, Aug 3.
- Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Medical Action Industries, Inc. 306 · Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
- Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Desc…
Oxos Medical Inc · Due to a defective circuit board that overheats
- Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
Innovasis, Inc · Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque…
- Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 F…
Maquet Critical Care AB · Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient re…
- Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2 Product…
Nuclein LLC · Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).
- STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
Stryker Corporation · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620
Stryker Corporation · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640
Stryker Corporation · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Stryker Corporation · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540
Stryker Corporation · There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
- Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475620 Product Description: Intramedullary Bone Saw Blade Assembly 12mm
Biomet, Inc. · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier pa…
- Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm
Biomet, Inc. · Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier pa…
Device clearances and approvals
FDA date:FDA decided 9 510(k)s and 6 PMA decisions on Mon, Jul 27.
- ND Needle Guidance System
Accurate Access, LLC · Radiology
- ARCHIMEDES Biodegradable Stent (Medium)
Q3 Medical USA, LLC (C/O Q3 Medical Devices Ltd.) · Gastroenterology, Urology
- FlexTract Deflectable-Rotational Dilator Sheath Set
Merit Medical Systems, Inc. · Cardiovascular
- Philips EPIQ Series Diagnostic Ultrasound System; Philips Affiniti Series Diagnostic Ultrasound System
Philips Ultrasound, LLC · Radiology
- Euphora Rapid Exchange (RX) Balloon Dilatation Catheter
Medtronic Ireland · Cardiovascular
- Powered Aventus Thrombectomy System
Inquis Medical · Cardiovascular
- Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave E8 Peripheral IVL Catheter
Shockwave Medical, Inc. · Cardiovascular
- Air Compression Massager (HY-1165)
Xiamen High Top Electronic Technology Co., Ltd. · Physical Medicine
- Intimate Rose Pelvic Wand (Purple); Intimate Rose Bendable Pelvic Wand (Orange); Intimate Rose Temperature Pelvic Wand (Yellow)
Plus EV Holdings, Inc. D/B/A Intimate Rose · Physical Medicine
Label updates
FDA date:154 drug labels took effect on Mon, Jul 27; 1 of the 25 read for this issue is for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.
- Liraglutide
LIRAGLUTIDE · Meitheal Pharmaceuticals Inc. · SUBCUTANEOUS
- Lamotrigine
LAMOTRIGINE · REMEDYREPACK INC. · ORAL
- aripiprazole
ARIPIPRAZOLE · REMEDYREPACK INC. · ORAL
- Mycophenolic Acid
MYCOPHENOLIC ACID · American Health Packaging · 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.
Subscribe with any feed reader, or point an email tool at the RSS feed to send each issue as a newsletter. Search any drug, device or company across every FDA dataset in the FDA data explorer.
