Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 17 minutes ago
United StatesMedline Industries, LP recalls Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.… and 15 more products
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.Ventec Life Systems, Inc. recalls VOCSN+Pro package
Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which may result…Zimmer, Inc. recalls Off-Axis Comprehensive Shoulder System Small and 4 more products
Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US…
Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process.Surgify Medical Oy recalls Surgify Halo and 18 more products
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).Sun Pharmaceutical Industries Inc recalls Perampanel CIII Tablets
Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets.ANI Pharmaceuticals, Inc. recalls hydrOXYzine Hydrochloride Oral Solution
Presence of foreign substancePReye LLC recalls PReye Vitamin See Antioxidant Preservative Free Eye Drops
Lack of Assurance of SterilityThe Harvard Drug Group LLC recalls Carton Label: MAJOR
Subpotent DrugCentral Admixture Pharmacy Services, Inc. recalls Total Parental Nutrition
Incorrect product formulation: bag did not contain copper and famotidine per label.Direct Rx recalls DULOXETINE D/R
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limitElevate Oral Care recalls Povi-One
sub potencyAjanta Pharma USA Inc recalls Fenofibrate Capsules
CGMP DeviationsCareFusion 213, LLC recalls BD ChloraPrep Clear and 3 more products
Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.Amgen, Inc. recalls Corlanor and 4 more products
Presence of Foreign Substance.Annora Pharma Private Limited recalls Lacosamide Tablets
Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.
CanadaAbiomed Introducer Kits with Impella Heart Pumps
Abiomed has initiated a voluntary medical device recall (correction) for all currently distributed Introducer kits that are used with Impella heart pumps to notify…Remifentanil hydrochloride for injection; Out of specification (Assay & Impurity)
The assay and impurity is out of specification in the affected lots.Spiriva Capsules ; Out-of-specification (uniformity of delivered dose)
The affected lot may not consistently provide the intended dose of medication with each use.Infinionâ„¢ CX Contact Lead Kit
Boston Scientific is initiating a voluntary removal of unused Infinionâ„¢ CX Leads as part of the planned transition to the next generation lead (Infinion Pro).UHI-4 High Flow Insufflation System - Insufflator
Olympus identified an increase in UHI-4 front-panel 'blackout' complaints, where the front-panel display turns off unexpectedly, and air delivery (insufflation) ceases.Argon Medical Devices L-Cathâ„¢ PICC and Midline Catheters
Reports of leaking and/or cracking at the hub of the affected products.Beta Bionics, Inc. recalls iLet Bionic Pancreas
The reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure could occur when the…A little guidance
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