Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 0 minutes ago
United StatesClariance-SAS recalls Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL…
Due to a quality issue regarding the presence of burr on the finished cervical plate product.Beta Bionics, Inc. recalls iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain…Philips Medical Systems Nederland B.V. recalls Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool).Therakos Development Limited recalls Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit…
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder.Wilson-Cook Medical Inc. recalls Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505. and 4 more products
Increased rate of out-of-specification endotoxin results.Gentuity, LLC recalls Gentuity HF-OCT Imaging System Model G10-01
The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx Prime…Remel, Inc recalls Yeastone Broth
Products may report incorrect AST results during quality control.Insulet Corporation recalls Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7
Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of being…ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift
An internal component of the actuators in a certain production batch may not meet the required mechanical strength.3B Medical, Inc. recalls React Health PHOENIX 5L Oxygen Concentrator
Devices which did not meet internal quality specifications were inadvertently distributed.Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Blemish Spot Treatment
Failed Stability SpecificationsAvantor Performance Materials LLC recalls Magnesium Chloride
Subpotent drugHuons Co., Ltd. recalls Lidocaine HCl injection and 3 more products
Lack of Assurance of SterilityThe Harvard Drug Group LLC recalls Memantine Hydrochloride Extended-Release
Failed Dissolution SpecificationsNephron SC, LLC recalls Albuterol Sulfate Inhalation Solution
Labelling: Illegible labelInternational Medication Systems Ltd. recalls EPINEPHRINE Injection
Lack of Assurance of SterilityApotex Corp. recalls Desmopressin Nasal Spray
Defective container: defect in a batch of bottle caps, specifically involving dislodged or missing cap liners.Cipla USA, Inc. recalls Cinacalcet Hydrochloride Tablets and 2 more products
CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limitPayless Compounders, LLC recalls Semaglutide-Glycine-Cyanocobalamin Injectable
Lack of Assurance of SterilityIsland Kinetics, Inc. d.b.a. CoValence Laboratories recalls Remedy Gel and 2 more products
Subpotent DrugOwen Biosciences Inc. recalls FHF Farmhouse Fresh and 3 more products
Chemical contamination: Presence of benzeneXiamen Kang Zhongyuan Biotechnology Co., Ltd. recalls exchange select and 14 more products
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility…A little guidance
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