Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 11 minutes ago
United StatesAVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Tyvek bag seal issue which may compromise sterility of the kit.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Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception)…Laerdal Medical Corporation recalls Laerdal Compact Suction Unit 4 RTCA version
units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21…Medline Industries, LP recalls Medline 14 Fr Suction Catheter Kits SKU DYND40972 and 1 more products
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter.Philips Medical Systems Nederland B.V. recalls Azurion 3 M12 System Model Numbers: and 7 more products
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.Medline Industries, LP recalls Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes… and 6 more products
These lots of reprocessed catheters may contain small particles of residual material.Philips North America Llc recalls Brilliance iCT and 3 more products
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry.Medline Industries, LP recalls Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK and 10 more products
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an…Surepulse Medical LTD recalls Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor and 4 more products
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.Elekta, Inc. recalls Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… and 1 more products
Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference.Meitheal Pharmaceuticals, Inc recalls Cetrorelix Acetate for Injection
Defective Delivery System: Missing or duplicated needles within the injection kitUnichem Pharmaceuticals USA Inc. recalls Doxazosin Tablets
Tablets/Capsules Imprinted with Wrong IDAmerisource Health Services LLC recalls Oxycodone Hydrochloride Tablets
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.Fresenius Kabi Compounding, LLC recalls acyclovir sodium and 4 more products
Lack of Assurance of SterilityPro Numb Tattoo Numbing Spray LLC recalls Pro Numb Tattoo Numbing Spray and 1 more products
cGMP deviationsF.H. INVESTMENTS, Inc. (dba Asteria Health) recalls ESTRADIOL and 24 more products
Presence of Foreign substance - potential presence of metal particulate matterMcKesson recalls UDENYCA
Temperature Abuse.
CanadaErbe 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…APO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
Affected lots were manufactured using an active ingredient that was out of specification for dissolution.Seasonique, Seasonale tablets: Affected lot(s) may not contain the correct amount of tablets (missing blister card)
Affected lot(s) may not contain the correct amount of tablets (missing blister card).Seasonique and Seasonale birth control pills are being recalled due to the possibility of a missing blister card
Teva Canada Ltd.A little guidance
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