Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 19 minutes ago
United StatesEmano Metrics, Inc. recalls Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is a…
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model was trained…Boston Scientific Corporation recalls Boston Scientific TheraSphere 360 Y-90 Management Platform
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input.Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.Kent Imaging, Inc. recalls SnapshotGLO Wound Imaging Device
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a…AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.Wilcox Industries Corp. recalls The intended use is to be paired with a weapon for aiming purposes.
Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units…Medline Industries, LP recalls MEDLINE ANTERIOR HIP and 2 more products
Medline Industries, LP is issuing a recall for specific Medline kits containing B.Paragon 28, Inc. recalls P28 PHANTON INTRAMEDULLARY NAIL SYSTEM
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology and 1 more products
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm…Medtronic Neurosurgery recalls Ventriculostomy Kit
Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the acceptable limit…Medline Industries, LP recalls Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES and 3 more products
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus…Ferno-Washington Inc recalls Power F2 Powered Fastening System
Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail.Medline Industries, LP recalls Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters and 8 more products
Affected kits contain recalled Bard Silastic Foley Catheters.Karl Storz Endoscopy recalls Flexible Hystero-Fiberscope Kits REF: 11264BBU1
Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for gynecology use…ICU Medical Inc. recalls Hotline Fluid Warming Set
ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent application at…Medline Industries, LP recalls MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF and 1 more products
The procedure kits contain ICU Medical, Inc.Boston Scientific Corporation recalls FARASTAR Ablation Generator EU and 2 more products
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.Medtronic MiniMed, Inc. recalls MiniMed Go App
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts…Alphatec Spine, Inc. recalls SafeOp Patient Interface
Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use…Penumbra, Inc. recalls Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Due to manufacturing issues, reperfusion catheters may fracturesAVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.Boston Scientific Corporation recalls FARASTAR Ablation Generator EU
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.Boston Scientific Corporation recalls FARADRIVE Steerable Sheath Clear IDE and 3 more products
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator…A little guidance
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