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 8 minutes ago
United StatesBeckman Coulter, Inc. recalls MicroScan Neg MIC 56 REF C42464 UDI-DI code: 15099590731212 MicroScan panels are…
Due to the likely presence of contamination in well(s).Koven Technology, Inc. recalls Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler
Product labeling includes a fetal indication for use that is not cleared under its 510(k).AMO Puerto Rico Manufacturing, Inc. recalls Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name…
Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as…Straumann USA LLC recalls Custom Abutment Ti and 1 more products
A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments.Navajo Manufacturing Company recalls Handy Solutions Neck & Shoulders Heating Pad
If heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by placing pad under the…Tandem Diabetes Care, Inc. recalls Tandem pumps are battery-operated infusion pumps capable of both basal and bolus…
The Czech language user guide contained multiple translation errors.Waldemar Link GmbH & Co. KG (Mfg Site) recalls Embrace Drill Tower and 1 more products
The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments.Medtronic MiniMed, Inc. recalls MiniMed" 780G
Three software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions 6.60, 6.61, and…CareFusion 303, Inc. recalls BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with…GE Medical Systems, LLC recalls Imactis CT-Navigation System
There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.Olympus Corporation of the Americas recalls Olympus Endoscope Suction Valve and 3 more products
The MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.Merit Medical Systems, Inc. recalls CentrosFLO Hemodialysis Catheters and 4 more products
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay…Olympus Corporation of the Americas recalls Brand Name: Olympus Everest Bipolar Cutting Forceps and 6 more products
Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process.Philips Ultrasound, Inc recalls Philips 3D6-2 Ultrasound Transducer and 10 more products
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.Erbe USA Inc recalls Flexible Cryoprobe and 2 more products
Probes may rupture/burst during activationPhilips Respironics, Inc. recalls Philips Respironics Trilogy Evo and 3 more products
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the…I.T.S. GmbH recalls Volar Radius Plate with Angular Stability with the following description: Radius Plate… and 16 more products
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).Orthalign, Inc recalls Drill Plate and 1 more products
Drill plates manufactured out of specification can result in a bone cut in excess 00800"(2.8448mm)Chiesi USA, Inc. recalls CUROSURF
Lack of Assurance of SterilityRadnostix recalls Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit
Failed Tablet/Capsule SpecificationsAmerisource Health Services LLC recalls Meclizine Hydrochloride Tablets
Failed tablet specifications.Macleods Pharma USA, Inc recalls Levothyroxine Sodium Tablets USP 150 mcg
Subpotent DrugTeva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension and 2 more products
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.A little guidance
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