FDA•
Fundamental Feed: 3 products
Fundamental Feed recalls three horse feed pellet products over elevated aflatoxin levels.
3 productsFilters
Category
Agency
Severity
Date
Distributed in
All Recalls
Back to home ←
FDA•MODERATEEXO Black Tattoo InkXtreme Inks recalls EXO Black tattoo ink due to Pseudomonas aeruginosa contamination.
FDA•MODERATEPhilips Brilliance CT SystemsPhilips recalls Brilliance CT systems due to scan trigger failure risking inadequate diagnosis and extra radiation.
3 products
FDA•MODERATEAMS Spinal KitWindstone Medical recalls AMS Spinal Kit (Part AMS13683A) due to supplier quality issues with included Lidocaine HCl injection.
8 products
FDA•MODERATEMedtronic EOPA Arterial CannulaMedtronic recalls EOPA 22 Fr arterial cannulae over pinhole leak risk during bypass.
6 products
FSIS•CRITICALRoyale and Top Valu Uncured BaconMaple Leaf Foods recalls 12,036 lbs of Royale and Top Valu uncured bacon over missing import reinspection.
2 products
FDA•MODERATEDorzolamide HCl and Timolol Maleate Ophthalmic SolutionMicro Labs recalls Dorzolamide HCl/Timolol Maleate 2%/0.5% 10mL ophthalmic solution due to defective container caps.
FDA•Proin ER TabletsPegasus recalls Proin ER 145mg tablets for dogs due to failed dissolution specs.
FDA•Ascend Laboratories: Multiple Dabigatran Etexilate CapsulesAscend recalls Dabigatran Etexilate Capsules (150 mg, 75 mg) over impurity/degradation failures.
3 products
FDA•MODERATEMan Fon: 2 productsMan Fon recalls Won Ton Wrappers over undeclared Yellow #5 and Yellow #6 allergens.
2 products
FDA•Mycophenolate Mofetil for InjectionMylan recalls Mycophenolate Mofetil for Injection 500 mg vials due to precipitate.
FDA•MODERATEL-Cath PICC S/L Peripherally Inserted Central CatheterArgon Medical recalls L-Cath PICC catheters (REF 384539, 384464, 384516, 384463) due to hub cracking risk.
2 products
FDA•MODERATEAMS Medical Convenience KitsWindstone Medical recalls 80+ AMS convenience kits over endotoxin risk in supplied sponges.
4 products
FSIS•CRITICALTasty Kitchen Chicken Noodle Condensed SoupBCI Foods recalls 4,300 lbs of Tasty Kitchen Chicken Noodle Soup imported without reinspection.
FDA•MODERATEFresenius Kabi: Multiple Rx Only ProductsFresenius Kabi recalls multiple injectable drugs due to hair found in product.
5 products
FDA•MODERATERohto-Mentholatum (Vietnam) Co: multiple drugsRohto-Mentholatum recalls multiple Rohto Cooling Eye Drops over sterility concerns.
8 products
FDA•Glycopyrrolate Oral SolutionPrecision Dose recalls Glycopyrrolate Oral Solution over an unidentified impurity.
FDA•MODERATEMedline Convenience Kits with BD PurPrep 26 mLMedline recalls convenience kits with BD PurPrep 26 mL over Bacillus contamination.
4 products
FDA•Cetirizine Hydrochloride Tablets 5 mgRising Pharma recalls Cetirizine HCl 5 mg tablets over Ranitidine cross-contamination.
FDA•MODERATEMedline Convenience Kits with Bard Silastic Foley CathetersMedline recalls convenience kits with Bard Silastic Foley Catheters over surface material risk.
9 products
FDA•CRITICALMedline HIP CDS-LF Convenience KitMedline recalls kits with Bupivacaine ampules over quality issues causing drug ineffectiveness.
2 products
FDA•MODERATEMiniMed Go AppMedtronic MiniMed recalls MiniMed Go App v1.0.0 and v1.1.0 over nighttime alert failure risking missed insulin doses.
FDA•MODERATEFlexible Hystero-Fiberscope KitsKarl Storz recalls hysteroscope kits with expired endoscopic seals that may compromise sterility.
FDA•MODERATESafeOp Patient InterfaceAlphatec Spine recalls SafeOp Patient Interface over software issue causing tEMG loss, system faults, and reboot prompts.
FDA•MODERATESnapshotGLO Wound Imaging DeviceKent Imaging recalls SnapshotGLO wound imaging devices due to battery charging failure.
FDA•MODERATEPipeline Flex Embolization Device with Shield TechnologyMicro Therapeutics recalls Pipeline Flex Embolization Device due to incorrect labeling of implant sizes.
2 products
FDA•CRITICALMedline Anterior Hip KitMedline recalls anterior hip kits with Bupivacaine injection due to quality issues.
3 products
FDA•MODERATEHalyard Standard Line Insertion PackAVID Medical recalls Halyard Standard Line Insertion Pack (Model PVHM234-01) over silicone seal defects causing leakage.
- Device RecallFDA•MODERATEEmano Flow v2.0.0
Emano Flow v2.0.0 recalled due to audio sampling mismatch causing biased flow rate and volume estimates.
FDA•MODERATETheraSphere 360 Y-90 Management PlatformBoston Scientific recalls TheraSphere 360 Y-90 Platform due to software anomaly causing incorrect dose calculations.
FDA•MODERATEOlympus High Flow Insufflation Unit UHI-4Olympus recalls UHI-4 insufflation unit over unexpected display shutdown and air delivery loss.
FDA•MODERATEAXP Processing Bag SetThermoGenesis recalls AXP Processing Bag Set, Model 8-5101, over stopcock particulates in sterile fluid path.
FDA•CRITICALOrganic Moringa PowderGreen Jeeva is recalling bulk 15kg bags of Organic Moringa Powder (code GJ96) due to potential Salmonella contamination.
FDA•MODERATEBrooklyn Roasting Company Cold Brew ConcentrateBrooklyn Roasting Company is recalling 2.5-gallon Cold Brew Concentrate due to the risk of Clostridium botulinum toxin formation.
FDA•MODERATEVentriculostomy KitMedtronic is recalling the Ventriculostomy Kit due to endotoxin levels that exceed safety limits for cerebrospinal fluid contact.
FDA•MODERATEPenumbra RED 68 Reperfusion CatheterPenumbra is recalling the RED 68 Reperfusion Catheter due to a manufacturing issue that may cause the device to fracture during use.
FDA•MODERATEWilcox BOSS Xe Aiming LasersWilcox is recalling all BOSS Xe aiming lasers to implement a safety-related software enhancement.
- Device RecallFDA•MODERATE3mensio Vascular Fenestrated Workstation Software
3mensio software may report inaccurate cardiovascular measurements when analyzing specific Philips 3D echo datasets.
FDA•MODERATESilent Nite Sleep ApplianceThe Silent Nite Sleep Appliance (Model SILNT) is being recalled because it lacks required FDA clearance.
FDA•MODERATEOlympus 4K UHD LCD MonitorOlympus is recalling the 4K UHD LCD Monitor (model OEV321UH) due to a potential connector fault that may cause image loss or abnormalities.
FDA•MODERATEFARADRIVE Steerable Sheath Clear IDEBoston Scientific is recalling the FARADRIVE Steerable Sheath Clear IDE due to potential valve damage that may cause air embolism.
4 products
FDA•MODERATEAVID Medical Eye Pack Convenience KitAVID Medical is recalling the Eye Pack convenience kit (Model LVEY27) due to an incorrect concentration of Betadine solution.
FDA•MODERATESeaSpine Polyaxial HeadSeaSpine is recalling the Polyaxial Head due to a manufacturing error that may cause the component to detach during surgery.
FDA•MODERATECyproheptadine Hydrochloride SyrupRising Pharma recalls Cyproheptadine HCl Syrup 2mg/5 mL due to crystallization and floating particles.
FDA•MODERATELevothyroxine Sodium 25 mcg TabletsMajor Pharmaceuticals is recalling Levothyroxine Sodium 25 mcg tablets due to subpotency.
12 products
FDA•MODERATEAmlodipine and Olmesartan Medoxomil TabletsAscend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets (10 mg/20 mg) due to failed dissolution specifications.
FDA•Trokendi XR 25mg CapsulesSupernus Pharmaceuticals is recalling Trokendi XR 25mg capsules due to failed dissolution specifications.
FDA•MODERATEVintage Roots Root Beer SyrupVintage Roots is recalling 8 oz Root Beer Syrup due to the presence of an unapproved food additive, sassafras bark.
- FDA•Ascend Laboratories: Multiple Dabigatran Etexilate Capsules
Ascend Laboratories is recalling 110 mg and 150 mg Dabigatran etexilate capsules due to failed impurity and degradation specifications.
2 products 
FDA•Divalproex Sodium Delayed-Release TabletsBionpharma is recalling 500 mg Divalproex Sodium Delayed-Release Tablets due to the presence of foreign tablets or capsules in the bottles.