Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 2 minutes ago
United StatesSiemens Medical Solutions USA, Inc recalls ARTIS icono ceiling. Model Number: 11328100.
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place.Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT and 3 more products
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.Insulet Corporation recalls Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.… and 2 more products
External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus…Carl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.Masimo Corporation recalls Radius VSM ECG pre-connected Set and 1 more products
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal…Medline Industries, LP recalls Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE and 14 more products
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM).Teleflex LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges
Due to out-of-specification, or potential out-of-specification, levels of endotoxinsBoston Scientific Corporation recalls CRE Pro Wireguided 6-8mm 240cm and 11 more products
Potential sterile breach of the pouches in which devices are packaged.Bard Access Systems, Inc. recalls OTP5000 THORA/PARA TRAY and 13 more products
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.Raysearch Laboratories Ab recalls RayCare 2024A SP1. Oncology Information Systems. and 1 more products
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a…Medline Industries, LP recalls Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH PACK… and 7 more products
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD).Remel, Inc recalls GC Agar Base
Reduced or no recovery of some strains of Neisseria gonorrhoeae.Boehringer Ingelheim Pharmaceuticals, Inc. recalls Synjardy XR Tablets
CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been used for a different…Lannett Company Inc. recalls Dextroamphetamine Saccharate
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.McKesson recalls Gemcitabine Injection
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.Accord Biopharma Inc recalls IMULDOSA
Lack of assurance of Sterility:Accord Healthcare, Inc. recalls Levothyroxine Sodium Tablets
Subpotent DrugLupin Pharmaceuticals Inc. recalls prednisoLONE Acetate Ophthalmic Suspension
Presence of Foreign SubstanceSun Pharmaceutical Industries Inc recalls Fexofenadine Hydrochloride Tablets
Failed Impurities/Degradation SpecificationsAsclemed USA Inc. recalls Accucaine and 1 more products
Lack of Assurance of SterilityCipla USA, Inc. recalls Cinacalcet Hydrochloride Tablets and 2 more products
cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).Lupin Pharmaceuticals Inc. recalls Glucagon Emergency Kit for Low Blood Sugar
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.CareFusion 213, LLC recalls BD ChloraPrep Hi-Lite Orange and 9 more products
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers…A little guidance
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