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 15 minutes ago
United StatesMidmark Corporation recalls Midmark IQecg Digital ECG and 1 more products
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.Hollister Ulc recalls Onli 17cm Hydrophilic Urethral Intermittent Catheter
Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to…Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT
Component labeling discrepancyGE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.1 and 3 more products
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer.American Contract Systems Inc recalls American Contract System Convenience Kit and 3 more products
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays.AVID Medical, Inc. recalls Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR… and 1 more products
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.Medline Industries, LP recalls Medline medical convenience kits and 3 more products
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential…Canon Medical System, USA, INC. recalls Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital…
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.Merge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS
Software issue may cause measurements to be displayed inaccurately.Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar…Olympus Corporation of the Americas recalls POWERSEAL 5 MM
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.Medline Industries, LP recalls Medline Hudson RCI and 2 more products
Neonatal and infant heated wire breathing circuits may experience sporadic failure.IMRIS Imaging Inc recalls ORT200 and 1 more products
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked…Medline Industries, LP recalls Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more products
Kits contain a potentially contaminated component which were recalled by the manufacturerApotex Corp. recalls Paxil CR
Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteriaB Braun Medical Inc recalls Lactated Ringer's Injection USP
Presence of Particulate matter.Fresenius Kabi USA, LLC recalls Tyenne
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.Church & Dwight Co., Inc. recalls Zicam
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testingMallinckrodt Hospital Products Inc. recalls Acthar Gel
Presence of particulate matter: glass and stopper pieceLupin Pharmaceuticals Inc. recalls Clobetasol Propionate Cream USP
Failed content uniformity specifications.Hikma Pharmaceuticals USA INC. recalls Ramipril Capsules USP
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).Accord Healthcare, Inc. recalls Levothyroxine Sodium Tablets and 11 more products
Subpotent DrugSDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068
Potential for electrical discharge from unit when unplugged.A little guidance
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