Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 9 minutes ago
Medtronic Neuromodulation recalls Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation and 1 more products
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.Bolton Medical Inc. recalls RelayPro Thoracic Stent-Graft System
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile.Abiomed, Inc. recalls Automated Impella Controller
Retrospective submission for following issues identified: 1.Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection and 6 more products
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including…GE Medical Systems Information Technologies Inc recalls GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL and 5 more products
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and…AbbVie Inc. recalls PRED MILD
Failed Stability SpecificationsAVEVA Drug Delivery Systems, Inc. recalls Nicotine Transdermal System Patch
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of…Hybrid Infusions Ltd. recalls Champagne Supernova 3x0.5g Pre-Roll due to packaging and labelling issue
The affected product is packaged in the wrong tube.Beauty Pie Super Healthy Hair Coconut Water Heat Shield Spray recall
Batch 3094A of this product presents a microbiological risk as testing has indicated that it loses efficacy over time, which may lead to the growth of Pseudomonas…Hizentra: The appearance is out of specification in the affected lot.
The appearance is out of specification in the affected lot.Relay®Pro Thoracic Stent-Graft System
Through post-market surveillance, Bolton Medical received complaints where the graft is unable to unclasp from the delivery system because the proximal clasp is…CRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters
Boston Scientific is initiating removal of CRE™ Wireguided and CRE PRO™ Wireguided balloon dilation catheters due to a potential sterile breach of the pouches in which…Volara System Patient Ciruit
Baxter Corporation is issuing an urgent medical device correction for Volara System patient circuits due to reports of air and medication leakage from the nebulizer cup…Omnipod® Insulin Management System - Omnipod®
The defect is related to tears on the external (exposed) soft cannula.GE Healthcare AW Server
Potential patient context synchronization issue.Hamilton Medical AG Breathing Set MRI
Certain lots of the expiratory valve set pre-assembled to the breathing circuit set, coaxial (see FSN) do not perform as intended.Rubicon Holdings Corp. recalls one lot of Simply Bare Organics BC Organic Blue Dream Pre-Rolls due to packaging and labelling issue
The affected products contain the wrong pre-rolls.Gore® Tag® Thoracic Branch Endoprosthesis Side Branch Component
Catheter separation of the Gore® Tag® Thoracic Branch Endoprosthesis (TBE) Side Branch (SB) component during clinical use.WendyLett 4Way
Certain units of WendyLett 4Way, 200 × 190 cm, with handles, may be affected by a material defect that could cause the fabric to tear in or adjacent to the seams.CORFLO* Safety PEG Kit With ENfit® Connector
This recall is initiated due to quality issues related to sterility assurance to certain lidocaine hydrochloride injection products.ICU Medical, Inc. recalls Oncology Kit w/60"
Oncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if the leak occurs…Tangent Endoscopy, LLC recalls Tangent Endoscopy
Affected devices exhibited fractures at the distal shaft tip without complete detachment.A little guidance
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