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 22 minutes ago
United StatesSiemens Medical Solutions USA, Inc recalls ARTIS pheno and ARTIS Icono biplane
During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient.Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24"
Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.Brahms GmbH recalls B¿R¿A¿H¿M¿S KRYPTOR compact REACT
Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to…Cook Incorporated recalls COOK MEDICAL Approach CTO-6 Micro Wire Guide and 17 more products
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.Medline Industries, LP recalls NAMIC Angiographic Syringe and 18 more products
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a…XTANT Medical Holdings, Inc recalls XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.Teva Pharmaceuticals USA, Inc recalls Isotretinoin Capsules and 1 more products
Superpotent and SubpotentPreferred Pharmaceuticals, Inc. recalls Artificial Tears Lubricant Eye Drops
Lack of Assurance of SterilityViatris, Inc. recalls Xanax XR
Failed Dissolution SpecificationsCipla USA, Inc. recalls Lanreotide Injection and 1 more products
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.GE Healthcare Ireland Limited recalls GE Healthcare Omnipaque and 1 more products
Presence of particulate matterTeva Pharmaceuticals USA, Inc recalls Clonidine Transdermal System and 2 more products
CGMP Deviations: use of an unapproved raw materialFresenius Kabi USA, LLC recalls 0.45% Sodium Chloride Injection and 13 more products
Lack of Assurance of SterilityFagron Compounding Services recalls norepinephrine Bitartrate and 4 more products
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
The dietary supplements contain iron, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act.Cardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within…Philips Medical Systems Nederland B.V. recalls Vue Motion V12. Product Number: 1017979.
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Surgical light assembly may not adequate support the weight of the ceiling cover.Medline Industries, LP recalls Sterile Radiology Procedure Kits
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.Summa Therapeutics, LLC recalls Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter…
Potential for the balloon in the device to not meet burst specifications.Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module
Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease…Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo and 3 more products
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.Reflexion Medical, Inc. recalls RefleXion X1 Radiotherapy System Model RXM1000
Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the…A little guidance
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