Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 14 minutes ago
Rising Pharma Holding, Inc. recalls Rising
Presence of Precipitate: medication was crystallizing and particles floating in the bottlePrecision Dose Inc. recalls Glycopyrrolate Oral Solution
Failed Impurities/Degradation SpecificationsAscend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications; Olmesartan Medoxomil content below specificationsAsclemed USA Inc. recalls Lidolog Kit
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scanBionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets
Presence of Foreign Tablets/CapsulesAscend Laboratories, LLC recalls Dabigatran etexilate Capsules and 1 more products
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total…Fresenius Kabi USA, LLC recalls Glycopyrrolate Injection and 4 more products
Presence of Particulate Matter: Hair was found in product Presence of Particulate Matter: Hair was found in productsSupernus Pharmaceuticals, Inc. recalls Trokendi XR
Failed Dissolution SpecificationsMajor Pharmaceuticals recalls Levothyroxine Sodium Tablets and 11 more products
Subpotent DrugRohto-Mentholatum (Vietnam) Co., Ltd. recalls Rohto Cooling Eye Drops ALL-IN-ONE and 7 more products
Lack of Assurance of SterilityHashmi Kajal Eyeliner recall
The product presents a serious chemical risk as it contains mercury, cadmium, arsenic and lead.IQecg® Digital ECG
Affected IQecg® plugin software may produce incorrect ECG waveforms and inaccurate heart-rate calculations.Oxygen 100%: Gas cylinders containing commercial grade oxygen
Gas cylinders containing industrial grade oxygen were delivered instead of medical grade oxygen to a customer.Blanketrol® II 115V and Blanketrol® III 115V
Gentherm Medical has received complaints of overheated circuit boards in 0.53% of distributed devices.Spacelabs Healthcare Xhibit® Central Station
Spacelabs Healthcare has concluded that the use of the previously distributed splitter (part number 010-1975-00) can have an adverse effect on product performance…Sphere-9™ Catheter
There have been forty-six (46) reported incident reports (none of which were from Canada) where patients with a Biotronik ICD experienced induced ventricular arrhythmia…Harmonic Arts Holy Basil Tincture; Out of Specification (total aerobic microbial count)
The total aerobic microbial count is out of specification in the affected lot.OverStitch™ Suture Cinch and Suture Cinch–Long
Boston Scientific is initiating removal of specific lots of OverStitch™ Suture Cinch and Suture Cinch-Long (collectively "Suture Cinch").ATTITUDE Bathroom Cleaner Disinfectant: Affected lot may be missing expiry date
Affected lot may be missing expiry date.HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P
Stryker has identified a limited number of HeartSine samaritan PAD devices that were distributed without the required maintenance supplement.DCA Vantage® HbA1c (DX Claim)
Siemens Healthineers has confirmed through customer complaint investigation and internal testing that delamination of the buffer pull-tab may occur in a small subset of…HeartSine® Samaritan® PAD SAM 350P/SAM 360P/SAM 500P - Membrane Tail
Stryker has recently identified an issue with the membrane tail, an internal component, which could cause an intermittent fault.3B Medical, Inc. recalls Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number…
Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).A little guidance
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