Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
225 recalls match · Clear filters · Checked 5 minutes ago
United StatesMedline Industries, LP recalls Medline Convenience Kits: 1) ANCILLARY PACK-LF and 41 more products
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices.
CanadaBioFlo Dialysis Catheter With Endexo Technology
Merit Medical Systems, Inc.
Maison Luce brand Sérum fortifiant Cils & Sourcils recalled due to chemical hazard
Health Canada's sampling and evaluation program has determined that the recalled product contains methyl eugenol above the maximum concentration in the Cosmetic…Intuitive Surgical, Inc. recalls da Vinci 5 Surgeon Console Viewer Display
Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception)…Erbe Flexible Cryoprobe
Erbe Elektromedizin Gmbh has been made aware of cases of Erbe Flexible Cryoprobes rupturing/bursting during activation.
Patchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients
It was determined that these products contained prohibited ingredients as per Health Canada’s Cosmetic Ingredient Hotlist (‘Hotlist’).
Haleine Fraîche oral hygiene product 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…Medline Kits containing Surgical Gowns, Packs and Drapes
Medline identified calibration issues linked to the equipment used to sterilize the recalled products, impacting the sterility assurance level.Boston Scientific Corporation recalls AXIOS Stent and Electrocautery-Enhanced Delivery System and 5 more products
Increased reports of stent deployment and expansion issues.cobas® pro and cobas® pure
A rare software malfunction has been identified on the cobas® pro (c503) and cobas® pure (c303) platforms affecting the calibration library.CareFusion 303, Inc. recalls BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System…
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital…Surgical Drapes, Packs, Gowns
Medline identified calibration issues linked to the equipment used to sterilize the recalled products, impacting the sterility assurance level.
Mindbodygreen Recalls Ultimate Multivitamin+ Dietary Supplement Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
The bottles are filled with dietary supplements containing iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.MOLLI 2 Systems
Stryker has updated the MOLLI 2 system Instructions for Use (IFU) following two medical device reports (MDRs) submitted to the FDA (June 5 2025).
Truly Tallow All-in-1 Mens Face + Body + Hair Whipped Tallow recalled due to a chemical hazard
Health Canada's sampling and evaluation program has determined that the recalled product contains methyl eugenol above the maximum concentration in the Cosmetic…Boston Scientific Corporation recalls Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter…Medtronic Inc recalls Abre Venous Self-Expanding Stent System
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force.Ge Medical Systems Israel, Functional Imaging recalls SMV DSX New Line and 3 more products
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in…Diagnostica Stago, Inc. recalls Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for…
Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results.Heraeus Medical GmbH (Dental Division) recalls Brand Name: PALACOS Product Name: PALACOS R pro 40 and 3 more products
increase of complaints regarding the breakage of the ampoules within their device systems.Philips Medical Systems Nederland B.V. recalls Product Name: Allura Xper FD10C and 15 more products
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or…
Lake of the Woods Sunrise Soap Co. Shades of Grey Bars of Soap 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…IMRIS Imaging Inc recalls Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number…
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