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 10 minutes ago
United StatesHaleon US Holdings LLC recalls Gas-X Extra Strength
Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.Ascend Laboratories, LLC recalls Minocycline Hydrochloride Extended-Release Tablets
Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysisBaxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number…
Affected lots may contain incorrect 0.8-micron filters.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be…Windstone Medical Packaging, Inc. recalls Aligned Medical AMS16835 Fluids Kit RX
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.Fresenius Kabi USA, LLC recalls LVP software of the Ivenix Infusion System
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the…GE Medical Systems Information Technologies Inc recalls CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Electrical sparking may occur at the printer head.Covidien, LP recalls Covidien EndoStitch" Polysorb Single Use Loading Unit
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.DeRoyal Industries Inc recalls DeRoyal Industries Inc. Ref 46-406
Sterile wound dressing, lacks sterility assuranceSSC- Surgical Specialties Corporation recalls Sharpoint 2.2MM
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.Shimadzu Medical Systems recalls Digital Angiography System Trinias:UD150G-40 / D150GC-40
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.Fresenius Kabi USA, LLC recalls The Large Volume Pump
Potential for the Cassette Loading Lever to break.Oculus Technologies of Mexico, S.A. de C.V. recalls PhaseOne Antimicrobial Solution
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component.Grace Medical, Inc. recalls TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product…
Due to incorrect functional length on device labeling.Siemens Medical Solutions USA, Inc recalls ARTIS pheno and 1 more products
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient.Covidien LLC recalls COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code…
Due to customer complaint regarding incorrect display box labeling.Advanced Bionics, LLC recalls Brand Name: HiResolution" Bionic Ear System Product Name: HiRes Ultra 3D CI HiFocus Mid…
Due to incorrect shelf-life expiration date.GE Medical Systems China Co., Ltd. recalls MAC 5 A4 Resting ECG Analysis System 855001-001
Software in development inadvertently made available for customer use.Daavlin Distributing Company recalls Phothera 200
Some of the Calibration/Output Certificates had the outputs reversed.Kayserbetten GMBH & Co. KG recalls Pediatric care bed
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an…Stryker Corporation recalls Neptune Smart Docking Station
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior…Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set and 1 more products
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.Intuitive Surgical, Inc. recalls Brand Name: Da Vinci 5 Product Name: ASSY
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when…A little guidance
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