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 StatesMedline Industries, LP recalls MEDLINE convenience kits labeled as LOCAL BASIC and 19 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils.Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.Imprimis NJOF, LLC recalls Klarity-C Drops
Subpotent DrugZydus Pharmaceuticals (USA) Inc recalls Bromocriptine Mesylate Capsules
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.Park Avenue Compounding recalls Fentanyl citrate
CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.Otsuka ICU Medical LLC recalls POTASSIUM CHLORIDE Inj. and 1 more products
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj.Golden State Medical Supply Inc. recalls NIACIN Extended-Release Tablets
Failed Dissolution SpecificationsDermaRite Industries, LLC recalls 4-N-1 Skin Protectant and 17 more products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.Stryker Sustainability Solutions recalls HARMONIC FOCUS Shears + Adaptive Tissue Technology
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.Siemens Medical Solutions USA, Inc recalls MAGNETOM Cima.X Upgrade. Model Number: 11689304.
There is a potential for an ice blockage to form or currently exist within the primary and/or the auxiliary venting paths of the magnet helium containment venting system.Shimadzu Corporation Medical Systems Division recalls Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed
Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.Becton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date.Orthofix U.S. LLC recalls Virata Preassembled Polyaxial Screw
Polyaxial screws do not meet performance standards.Miach Orthopaedics recalls BEAR Implant
The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk stock only.NeuroLogica Corporation recalls GM85 Digital Mobile X-ray imaging System
The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.Sonesta Medical AB recalls Brand Name: Sonesta Product Name: 6210 Model/Catalog Number: 0120-LA120-03 Software…
Video fluoroscopy table may contain inadequate weld on backrest bracket resulting in backrest dropping.Abbott Laboratories recalls Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number…
Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results.Olympus Corporation of the Americas recalls Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use… and 1 more products
Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.Abbott Medical recalls Eterna SCS IPG and 1 more products
There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS)…Accriva Diagnostics, Inc. recalls VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The…
Due to an device without a premarket clearance being incorrectly package and distributed.Siemens Healthcare Diagnostics, Inc. recalls IMMULITE 2000 Oak Mix Specific Allergen and 2 more products
The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge.Philips Respironics, Inc. recalls SimplyGo Mini
Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output…Medline Industries, LP recalls Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits and 9 more products
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing.A little guidance
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