Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 8 minutes ago
United StatesPermobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031
This recall has been reported retroactively.Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga and 1 more products
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may…Philips Medical Systems recalls Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000… and 2 more products
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually.Terex Utilities recalls Power Over Fiber Base Module
Device not certified - no laser product report was filed with CDRH prior to distribution.IsoTis OrthoBiologics, Inc. recalls OsteoBallast
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with…Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack and 3 more products
The recall notice was initiated due to a Medicom Urgent Medical Device Recall.ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides…
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of…Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR and 5 more products
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass.Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030. and 6 more products
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.Instrumentation Laboratory recalls GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with… and 2 more products
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KIT and 7 more products
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP.Micro Labs USA Inc recalls Dorzolamide HCl and Timolol Maleate Ophthalmic Solution
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.Mylan Pharmaceuticals Inc recalls Mycophenolate Mofetil for Injection USP
Presence of precipitateGlenmark Pharmaceuticals Inc., USA recalls Azelaic Acid Gel
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.Ascend Laboratories, LLC recalls Dabigatran Etexilate Capsules and 2 more products
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month…
CanadaNeedle Kit For Powered Driver
Some lots were manufactured with out-of- tolerance dimensions, and as a result some users have reported difficulty removing the obturator (stylet) following placement…
United KingdomRIEMANN P20 Hyperpigmentation Defence Face Cream SPF50+ 50g sold by Next recall
The specific batches of this product sold by Next were found to be past their expiry date.Pharmasave Regular Strength Dairy Digestive Supplement Lactase Enzyme: Affected lot is labelled with the incorrect Natural Product Number (NPN) on the carton.
Affected lot is labelled with the incorrect Natural Product Number (NPN) found on the carton.Femyso: Affected lot may contain two green Mifepristone cartons or two pink Misoprostol cartons instead of one of each.
Affected lot may contain two green Mifepristone cartons or two pink Misoprostol cartons instead of one of each.Azurion Systems
Philips has identified two software-related issues affecting Azurion R2.x.10, R3.0, R3.1 and R4.0 systems that may result in delay of therapy, procedural complications…Olympus Corporation of the Americas recalls Olympus 4K UHD LCD Monitor. Model Number: OEV321UH. An electrically powered visual…
Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities.Prismatik Dentalcraft, Inc. recalls Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Model/Catalog Number…
Due to device not having FDA ClearancePIE Medical Imaging B.V. recalls 3mensio Workstation
User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than the actual…A little guidance
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