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 StatesMentor Texas LP recalls SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe
A single lot of expired syringes were distributed due to a distribution system control failure.Covidien LLC recalls Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060…
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog…
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible.Siemens 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 SterilityA little guidance
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