Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 17 minutes ago
Canada
United StatesCardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within…Philips Medical Systems Nederland B.V. recalls Vue Motion V12. Product Number: 1017979.
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Surgical light assembly may not adequate support the weight of the ceiling cover.Medline Industries, LP recalls Sterile Radiology Procedure Kits
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.Summa Therapeutics, LLC recalls Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter…
Potential for the balloon in the device to not meet burst specifications.Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module
Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease…Philips Respironics, Inc. recalls Philips Respironics Trilogy Evo and 3 more products
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.Reflexion Medical, Inc. recalls RefleXion X1 Radiotherapy System Model RXM1000
Due to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll corrections applied in the…Ultradent Products, Inc. recalls Jiffy Original Composite Polisher Cups
Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.ReCor Medical Inc. recalls Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿…
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.Abiomed, Inc. recalls Purge Cassette
Increased risk of purge leaks with Generation 1 purge cassettes.Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR and 1 more products
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Enzymatic Hemoglobin A1c
A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer.Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE… and 1 more products
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to…Abiomed, Inc. recalls Automated Impella Controller
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*)…Oxoid Australia Pty Limited recalls OXOID MICROBACT IDENTIFICATION KITS
Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result…BD Kiestra Lab Automation recalls BD Kiestra" ReadA
In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface.Synthes (USA) Products LLC recalls 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. and 1 more products
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect…Intuitive Surgical, Inc. recalls Brand Name: da Vinci S and 3 more products
Due to increased complaints for broken/frayed grip cables for reusable instruments.Philips Medical Systems Nederland B.V. recalls Allura Xper FD10C and 21 more products
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.Mentor Texas, LP. recalls CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 and 6 more products
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.Burlington Medical, LLC recalls Burlington Medical and 12 more products
Potential for attenuation degradation over time, decreasing the lifespan.Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 12G and 7 more products
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers.A little guidance
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