Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 20 minutes ago
United StatesMedtronic 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…JB Chemicals and Pharmaceuticals Ltd recalls Cetirizine Hydrochloride Tablets USP 5 mg
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg.Rising Pharma Holding, Inc. recalls Rising
Presence of Precipitate: medication was crystallizing and particles floating in the bottlePrecision Dose Inc. recalls Glycopyrrolate Oral Solution
Failed Impurities/Degradation SpecificationsAscend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications; Olmesartan Medoxomil content below specificationsAsclemed USA Inc. recalls Lidolog Kit
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scanBionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets
Presence of Foreign Tablets/CapsulesAscend Laboratories, LLC recalls Dabigatran etexilate Capsules and 1 more products
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total…Fresenius Kabi USA, LLC recalls Glycopyrrolate Injection and 4 more products
Presence of Particulate Matter: Hair was found in product Presence of Particulate Matter: Hair was found in productsSupernus Pharmaceuticals, Inc. recalls Trokendi XR
Failed Dissolution SpecificationsA little guidance
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