Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 0 minutes ago
CanadaEdan Patient Monitors
Labeling issue: an inappropriate publicly routable IP address was used as an example in IFU for demonstrating user-configurable IP address settings.Hot AXIOSâ„¢ Stent And Electrocautery-Enhanced Delivery System
Boston Scientific is initiating a removal of certain AXIOS™ Stent and Electrocautery Enhanced Delivery Systems (6 mm × 8 mm, 8 mm × 8 mm, and 20 mm × 10 mm).Econo Sterile™ instruments
Sklar instruments is voluntarily recalling certain lots of its Econo Sterileâ„¢ instruments.
United KingdomWet n Wild Proline Felt Tip Eyeliner E8752 recall
The product presents a serious chemical risk as it was found to have a concentration level of 11.5% Carbon Black (nano) colour pigment, which exceeds the maximum…Embark My Freedom and Embark My Story Perfumes safety warning
The products present a serious chemical risk as they contain butylphenyl methylpropional (BMHCA/lilial), which is prohibited in cosmetic products.Broselowâ„¢/Hinkle Pediatric Emergency System Sets
AirLifeâ„¢ has identified three medication-related errors in the content printed on the affected product version of the AirLifeâ„¢ Broselowâ„¢ Rainbow Tape.Suture/Laceration Tray by Canadian Hospital Specialties Ltd.
The recall is due to a labeling error affecting the Laceration Tray MRX.Mazorâ„¢ X System
Mazor software version 5.2 is an update to any prior software version, including software versions 5.0.1, 5.1.2, and 5.1.3.
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.Azurion R3.0 Systems
Philips has identified nine software issues affecting Azurion R3.0 systems that may result in loss of imaging (X-ray) functionality, and/or loss of motorized movement…Achieva 3.0T MRI System-Main Unit
Philips has become aware through in-house testing of a potential safety issue affecting MR systems operating on software versions R11.1 to R12.1 that could pose a risk…Teva-Topilene Ointment 0.05%: The assay is potentially out of specification in the affected lot during its shelf life.
The assay is potentially out of specification in the affected lot during its shelf life.Viazen Immunity: The selenium content is out of specification in the affected batch.
The (selenium) content is out of specification in the affected batch.
Mira Henna Cones recalled due to chemical hazard
The recalled products contain phenol which is a prohibited Hotlist ingredient.Sentinel V11 (Sentinel Cardiology Information Managment System)
Spacelabs Healthcare identified two issues with version 11.6.0 that can result in incorrect patient data being associated with clinical reports, potentially resulting…IMRIS HFD100 Head Fixation Device
IMRIS is conducting a voluntary recall to address a potential safety risk associated with use of the HFD100 Head Fixation Device and will be completing corrective…APO-TRAVOPROST-TIMOP PQ: missing the documented justification for the results obtained.
The affected lot is missing the documented justification for the results obtained.Aesculap Inc. Surgical Instrument Sets
AIC has become aware of the sales and distribution of certain medical devices into the Canadian market without a medical device license from Health Canada.Raz-AT, Raz-CAT, Raz-AP, Raz-SP (Mobile Shower Commode Chairs)
Raz decided a safety enhancement action that we are implementing for the Front and Rear Open (FAR) seats.
United StatesNipro Medical Corporation recalls Hemodialysis System
Screw may loosen or fallout of Hemodialysis systemMedline 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.Waldemar Link GmbH & Co. KG (Mfg Site) recalls Endo Model Knee Fusion Nail SK
The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.A little guidance
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