FDA daily for Wednesday, May 29, 2024
In this issue: 8 approvals, 8 drug recalls, 4 device recalls, 16 device decisions, 89 label changes and 7 food or supplement recalls. 2 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.
- Sildenafil Citrate
SILDENAFIL · NuCare Pharmaceuticals,Inc. · ORAL
Drug and biologic approvals
FDA date:On Wed, May 22 FDA approved 3 new applications (0 brand or biologic, 3 generic) and 5 supplements to existing ones.
- CEFEPIME HYDROCHLORIDE
HIKMA · CEFEPIME HYDROCHLORIDE
- DABIGATRAN ETEXILATE MESYLATE
MSN · DABIGATRAN ETEXILATE MESYLATE
- IRBESARTAN
IPCA LABS LTD · IRBESARTAN
Drug recalls
FDA date:FDA's enforcement report dated Wed, May 22 lists 8 drug recalls: 1 Class I, 7 Class II.
- Schwinnng Herbal Dietary Supplement Capsules, packaged in 10-count boxes, distributed by VSD Productions Inc., Las Vegas, NV.
Stop Clopez Corp · Marketed Without An Approved NDA/ANDA
- Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, In…
Lupin Pharmaceuticals Inc. · Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
- Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass jars, Gordon Laboratories, Upper Darby PA 19082, NDC 10481-3009-01
Dercher Enterprises, Inc., DBA Gordon Laboratories · cGMP Deviations
- MethylPREDNISolone Acetate Injectable Suspension, USP, 400 mg per 10 mL (40 mg per mL), 1 x 10 mL Multi-Dose Vial, Rx only, Mfd. for SAGENT…
Sagent Pharmaceuticals · Presence of Particulate Matter: Potential for black particulates in the drug product.
- Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution In…
Pharma Nobis LLC · Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
- CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Cherry Flavor, 10 fl. oz bottle, Distributed by: CVS Pharmacy, Inc., On…
Pharma Nobis LLC · Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria
- Losartan Potassium and Hydrochlorothiazide Tablets, USP 50mg /12.5 mg, 1000-count bottle, Rx only, Manufactured for: Macleods Pharma USA, I…
MACLEODS PHARMA USA, INC · Presence of foreign substance: plastic-like substance.
- Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, In…
Lupin Pharmaceuticals Inc. · Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Device recalls
FDA date:FDA posted 4 device recalls from 4 firms on Wed, May 22.
- SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Ethicon, Inc. · Some applicator tips from these lots had open seals.
- Cascade IOMAX Cortical Module, REF: 190296-200
Cadwell Industries Inc · There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly which could result in arcing to patient connections…
- Stryker Blueprint Software, Catalog #BPUE001.
Tornier S.A.S. · The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations t…
- Noblus AC Adapter used with the Noblus Ultrasound Imaging System Model : AHM250PS24
FUJIFILM Healthcare Americas Corporation · AC adapters of Noblus can heat up, and cause smoke in the worst case, when an excessive mechanical stress is applied to the socket for power cable (frequent in…
Device clearances and approvals
FDA date:FDA decided 10 510(k)s and 6 PMA decisions on Wed, May 15.
- BriefCase-Quantification
Aidoc Medical , Ltd. · Radiology
- BruxZir® NOW SRC
Prismatik Dentalcraft, Inc. · Dental
- Full Wedge Lateralized and Augmented Baseplates
Fx Shoulder USA, Inc. · Orthopedic
- CANON Fundus Camera CR-10 (CR-10)
Canon, Inc. · Ophthalmic
- Heuron ICH
Heuron Co., Ltd. · Radiology
- TRIUX neo (NM27000N ); MEGreview (SW26241N-B)
Megin OY · Neurology
- E3D-A Interbody System
Evolution Spine · Orthopedic
- Notal Vision Home Optical Coherence Tomography (OCT) System
Notal Vision, Inc. · Ophthalmic
- Augment Off-Axis Instrument System
Fix Surgical · Orthopedic
Label updates
FDA date:89 drug labels took effect on Wed, May 15; 6 of the 25 read for this issue are for products in MedGrid's categories. Below: those, and labels carrying a boxed warning.
- Sildenafil Citrate
SILDENAFIL · NuCare Pharmaceuticals,Inc. · ORAL
- LYLLANA
ESTRADIOL · Amneal Pharmaceuticals LLC · TRANSDERMAL
Food and supplement recalls
FDA date:FDA's enforcement report dated Wed, May 22 lists 7 food or supplement recalls: 2 Class I, 3 Class II, 2 Class III.
- Sensible Portions brand Garden Veggie Straws Sea Salt. 1 oz bag UPC:2951530057 Packaged in a 30 CT Variety Pack that contains Sea Salt, Che…
THE HAIN CELESTIAL GROUP INC · Undeclared milk
- Infinite Herbs Organic Basil packed in a clear 2.5 oz, 2.0 oz, and 4 oz PET clamshell container.
Infinite Herbs, LLC · Salmonella typhimurium in organic basil
- Sysco Classic Riced Cauliflower packed in a 4lb plastic bag (6 units of 4 lb. per carton box).
CN Frozen Foods, INC · Riced Cauliflower tested positive for Listeria monocytogenes.
- Savor brand Spicy MANGO slices; net weight 8.0 oz. (227 grams)
Savor Fine Foods · Product contains undeclared hydrolyzed soy protein.
- Jalapenos packed in 6lb 10oz cans. 6 cans per case
M-C McLANE INTERNATIONAL · Glass contamination
- 1. Country Club, Price Chopper, Good & Gather, Hiland, Belfonte, Great Value, Hen House Vitamin D Whole Milk, 1 gallon. 2. Country Club, Pr…
Hiland Dairy Foods Company, LLC · May contain potable water.
- Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 tea bag, 16 tea bags per pack, 4 packs per box. UPC on bo…
East West Tea Company, LLC · Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.
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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