Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
225 recalls match · Clear filters · Checked 6 minutes ago
The Paris Apothecary Aristocrat Beard Oil and Beard Balm recalled due to a chemical hazard
Health Canada’s sampling and evaluation program has determined that the recalled products contain methyl eugenol above the maximum concentration outlined in the…ShockPulse Lithotripsy System, Generator and Transducer
Olympus has identified instances of ShockPulse generator remaining in a blinking phase waiting to recognize the transducer following previous FY26-010 recall.Cook Incorporated recalls Flexor Check-Flo Introducers and Sets and 2 more products
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade… and 16 more products
Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture.Fresenius Medical Care Holdings, Inc. recalls 5008X CAREsystem +CLiC +CDX
Several software anomalies with the potential to impact patient treatment, of which one includes the possibility to result in treatment stop if certain conditions are…Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray… and 5 more products
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.Asserachrom® HPIA
After receiving three customer complaints (from outside Canada and the US), Stago investigated and confirmed that approximately 5% of reagent 1 strips had a defect for…Elecsys® Anti-TSHR
Internal reviews have confirmed two related problems with the Elecsys® Anti-TSHR assay.Econo Sterile™ instruments
Sklar instruments is voluntarily recalling certain lots of its Econo Sterile™ instruments.Suture/Laceration Tray by Canadian Hospital Specialties Ltd.
The recall is due to a labeling error affecting the Laceration Tray MRX.BEB Bubbly Wash recalled due to microbial contamination
The recalled products can contain the bacteria Klebsiella aerogenes.Rifton TRAM and E-Pacer
Rifton initiated recalls for TRAM and E-Pacer units due to an unrelated buckle spring failure, which led to replacing the full body support strap assembly.Mira Henna Cones recalled due to chemical hazard
The recalled products contain phenol which is a prohibited Hotlist ingredient.Medline Industries, LP recalls MEDLINE PERFUSION SYRINGE
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps.Bard Peripheral Vascular Inc recalls Safe-T-Centesis 6 Fr Catheter Drainage Tray
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show…Accriva Diagnostics, Inc. recalls Hemochron Activated Clotting Time Low-Range Test Cuvette
Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected…Fresenius Kabi USA, LLC recalls IVENIX INFUSION SYSTEM
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.Paragon 28, Inc. recalls Phantom Fibula Nail
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be…Zeus Infinity Empowered (Anesthesia Workstation)
The action is being initiated due as a cybersecurity vulnerability was discovered as part of an internal SW penetration test.Flexor® Check-Flo Introducer and Rösch-Uchida Transjugular Liver Access Sets
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.FreeStyle Libre® 3 Plus Sensor Kit
A subset of FreeStyle Libre® 3 plus sensors may provide incorrect low glucose readings.Medtronic Sofamor Danek USA Inc recalls Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding…
Expandable interbody system cage may loose height or collapse (loss of lordosis), which could result in migration, subsidence and/or neurological injury.Intelerad Medical Systems Incorporated recalls IntelePACS
Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss…A little guidance
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