Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 18 minutes ago
United StatesLannett Company Inc. recalls Niacin Extended-release Tablets
Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.Asclemed USA Inc. recalls Duloxetine DR Capsules
CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications: Olmesartan Medoxomil content below specificationsSun Pharmaceutical Industries Inc recalls Xyvona and 1 more products
Labeling: Not Elsewhere Classified.Eugia US LLC recalls Lidocaine HCl Injection
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scanSpectra Medical Devices, Llc recalls Lidocaine HCl Injection USP
Lack of Assurance of SterilityGuardian Drug Co. Inc. recalls KIRKLAND Signature and 22 more products
Presence of foreign substance: small metallic particles in chewable tablets.
CanadaGuedel Airway
During manufacture, some devices have been identified with occluded or partially occluded tips of the Guedel Airway.PMS-Fluconazole 50 mg tablets; Incorrect quantity of tablets
The affected batch may not contain the correct quantity of tablets.Baxter Corporation products recall; Blue cap breakage
Blue Caps Enhanced Closures (blue tip protectors) may break apart in affected lots.
Renpure Tea Tree & Rosemary Scalp Rebalancing Shampoo & Conditioner recalled due to microbial contamination
These lot codes have elevated microbial levels including aerobic bacteria count, yeast/mold count and Burkholderia cepacia complex which may cause irritation and…Harmony™ Delivery Catheter System
Medtronic had received two (2) complaints about Harmonyâ„¢ DCS distal tip detachment during the implant procedure.Philips Allura Xper Systems
Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended…Giraffe™ OmniBed™ Carestation™
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device.
SpainYodeyma eau de toilette recall: chemical risk
The product contains benzyl alcohol, but the presence is not indicated in the list of ingredients.ARTIS Icono Ceiling, Floor and Biplane Systems
In very rare situations, after increasing the detector lift height to its maximum or minimum, the system may lose its movement capability.Dexcom G7 Sensor 1 Pack
Unauthorized third-party distribution of 2 Dexcom G7 sensor lots in Canada that were intended for destruction as they did not meet Dexcom product standardsIntelliCuff®
An issue was identified where the affected IntelliCuff® devices may alarm with "cuff system leakage", the motor pumps continuously and does not maintain the cuff…BD Canada ChloraPrep product recall; Sterility concerns
Product sterility is compromised in affected lots.IceMan CLASSIC3â„¢
Complaints received reporting a consistent failure mode described as a broken connector on IceMan CLASSICâ„¢ cube unit.Abiomed, Inc. recalls Automated Impella Controller
A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns.Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker
Incorrect inner package labeling.O&M Halyard Inc recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771
Nitrile Exam Glove failed to meet specifications chemical permeation performance.A little guidance
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