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 0 minutes ago
United StatesSun Pharmaceutical Industries Inc recalls Carbamazepine Tablets
CGMP Deviations; black spots found on tablets from burnt excipient during manufacturingFresenius Kabi USA, LLC recalls Morphine Sulfate Injection
Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.Mylan Pharmaceuticals Inc recalls Acamprosate Calcium
Failed Dissolution SpecificationsRegeneron Pharmaceuticals Inc recalls Libtayo
Lack of Assurance of SterilityShilpa Medicare Limited recalls PEMRYDI RTU and 1 more products
Discolored solution.Golden State Medical Supply Inc. recalls Carbamazepine Tablets
CGMP deviations: tablets with black specks.American Regent, Inc. recalls Nitroglycerin injection and 11 more products
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde Presence of Particulate Matter: Product…Philips Medical Systems Nederland B.V. recalls Philips Azurion Rystem
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or…BioFire Diagnostics, LLC recalls BIOFIRE Respiratory Panel 2.1
Due to increase in false negative resultsOBP Medical Corporation recalls OBP Medical
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions for both the patient…Bioporto Diagnostics A/S recalls ProNephro AKI
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate…Straumann USA LLC recalls GM Helix Implant
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label.Waldemar Link GmbH & Co. KG (Mfg Site) recalls Endo-Model
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau.BD Switzerland Sarl recalls 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext…
Products may not have received adequate sterilization processing.Spacelabs Healthcare, Inc. recalls Brand Name: Xhibit Product Name: Xhibit Central Station Model/Catalog Number: 96102…
Due to off-the-shelf display port component that has audio/video failuresStraumann USA LLC recalls Straumann Bone Level Tapered
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling…Erbe USA Inc recalls ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
A strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector resulting in CO2…Philips Medical Systems Nederland B.V. recalls Philips Azurion
Two software related issues: 1) Potential image quality degradation that may lead to delay of therapy, procedural complications and/or inappropriate treatment and 2)…Remel Europe Ltd. recalls Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL
Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.Ventana Medical Systems, Inc. recalls navify Digital Pathology
Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer windowGalt Medical Corporation recalls Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP
Black depth markings may detach from the outer sheath of the coaxial dilator introducer component of transcarotid-peripheral access kits.Baxter Healthcare Corporation recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position.Spectra Medical Devices, Llc recalls Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection
Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance.A little guidance
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