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 6 minutes ago
United StatesWinder Laboratories, LLC recalls Morphine Sulfate Oral Solution 100 mg / 5 mL
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.Dr. Reddy's Laboratories, Inc. recalls Varenicline Tablets
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.Cipla USA, Inc. recalls Lanthanum Carbonate chewable tablets and 1 more products
Failed stability specifications: Out of specification for hardness testAccriva Diagnostics, Inc. recalls Hemochron Activated Clotting Time Low-Range Test Cuvette
Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected…Illumina, Inc. recalls Reagent Kits/ containing flow cells
An instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow cell gaskets that have…Enterix, Inc. recalls InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit
InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.Medtronic, Inc. recalls Aurora EV-ICD and Clinical EV-ICD
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.Aizu Olympus Co., Ltd. recalls Olympus OER-Elite and 2 more products
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct…Fresenius Kabi USA, LLC recalls IVENIX INFUSION SYSTEM
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.Microbiologics Inc recalls KWIK-STIK
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.Siemens Medical Solutions USA, Inc recalls MAMMOMAT Revelation and 2 more products
There were instances where the operator table was sold together with a bus-installation kit.Paragon 28, Inc. recalls Phantom Fibula Nail
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be…Philips North America Llc recalls Incisive CT and 1 more products
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.Baxter Healthcare Corporation recalls Welch Allyn INF BAG
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the…Philips Ultrasound, LLC recalls Lumify Diagnostic Ultrasound System models : 795005
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.Get Tested International Ab recalls Alcohol and 87 more products
Distribution without premarket approval/clearance.Philips North America Llc recalls IntelliVue MP2. Product Number: M8102A. and 21 more products
Potential issue where the IntelliVue monitors did not alarm.Cipla Limited recalls Phytonadione Injectable Emulsion
Failed Stability Specifications: Observed OOS results: eg results for colour indexTeva Pharmaceuticals USA, Inc recalls Carton label: Testosterone Gel 1%
Defective Container - A defect in the side-seal which allows leakage of product.Breckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules and 1 more products
CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limitPark Avenue Compounding recalls Phenylephrine HCI
CGMP DeviationsSafecor Health, LLC recalls Haloperidol Lactate Injection
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.A little guidance
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