Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 6 minutes ago
United StatesThoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System and 3 more products
Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100
If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump…Cellavision AB recalls REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60
Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic results.ASP Global, LLC. dba Anatomy Supply Partners, LLC. recalls SAFE-T-FILL Micro Capillary Blood Collection and 23 more products
Due to products manufactured under an inadequate quality system to include unvalidated manufacturing processes.Medline Industries, LP recalls MEDLINE convenience kits labeled as LOCAL BASIC and 19 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils.Alembic Pharmaceuticals Limited recalls Fesoterodine Fumarate
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.Imprimis NJOF, LLC recalls Klarity-C Drops
Subpotent DrugZydus Pharmaceuticals (USA) Inc recalls Bromocriptine Mesylate Capsules
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.Park Avenue Compounding recalls Fentanyl citrate
CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.Otsuka ICU Medical LLC recalls POTASSIUM CHLORIDE Inj. and 1 more products
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj.Golden State Medical Supply Inc. recalls NIACIN Extended-Release Tablets
Failed Dissolution SpecificationsDermaRite Industries, LLC recalls 4-N-1 Skin Protectant and 17 more products
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
CanadaExtra Strength Ibuprofen Liquid Gel Capsules: Presence of cloudy capsules in affected lots
Presence of cloudy capsules in affected lots due to crystallization of ibuprofen into the gelatin shell.
United KingdomArko Comfort After Shave Cologne safety warning
The product presents a serious chemical risk as it contains butylphenyl methylpropional (BMHCA), which is prohibited in cosmetic products.PMS-QUETIAPINE: Out of Specification
The content (quetiapine) is out of specification in the affected batches.Viewpoint 6
The patient history tab in Viewpoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information.Syrex Flush Syringe With Sodium Chloride
Medline was informed that a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.T7 Zipper Toga
Some shipments of the surgical device shipped already expired, potentially compromising their sterility.JAMP-Risperidone 0.25mg: Out of specification (Stability)
The impurities are out of specification during stability in the affected lots.Xpert® BCR-ABL Ultra
Using Xpert® BCR-ABL Ultra test kits with specimens that have markedly elevated white blood cell count (>30,000 cells/μl) may in rare circumstances cause inaccurate…Med-Rx Paracentesis Tray and Med-RX Drainage Tube
CHS has been made aware of some concerns related to the above products where some hospitals/facilities protocols involve the use of alcohol or alcohol-based drugs on…Elekta Modulator Discharge Rod
Elekta has identified a safety concern related to the modulator discharge rod.Stryker Sustainability Solutions recalls HARMONIC FOCUS Shears + Adaptive Tissue Technology
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.A little guidance
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