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Cyclophosphamide for Injection
Sunny Pharmtech recalls Cyclophosphamide for Injection over steel particulate matter in 3 lots.
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FDA•Cefazolin in Dextrose Injection 2g/100mLBaxter recalls Cefazolin in Dextrose Injection 2g/100mL over particulate matter (cardboard) in solution.
FDA•Papaverine Hydrochloride Injection 60 mg/2 mLAmerican Regent recalls Papaverine HCl Injection 60 mg/2 mL over visible particulate matter.
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
FDA•Midwest Poultry Shell EggsMidwest Poultry recalls Kroger, Simple Truth, and Brookshire's shell eggs over Salmonella risk.
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.
NHTSA•MODERATECoach and Equipment Phoenix/Metrolite Wheelchair LiftCoach and Equipment recalls Phoenix/Metrolite buses with S-Series wheelchair lifts due to contactor failure that may prevent stopping.
NHTSA•MODERATEATC RM500 and RM700 Winch RemoteATC recalls 2026 RM500 and RM700 trailers over winch remote incompatibility that may cause unexpected movement.
FDA•Pumpkin Tree Peter Rabbit Organics Banana & Strawberry Fruit Puree PouchesPT Organics recalls Pumpkin Tree Peter Rabbit Organics Banana & Strawberry Fruit Puree Pouches over possible soft plastic contamination.
FDA•Spicy Breakfast BurritosFresh & Ready Foods recalls Spicy Breakfast Burritos over undeclared soy allergen.
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•LOWShandong Ling Xian Food Co: 3 productsShandong Ling Xian Food is recalling three imitation crab products due to undeclared sodium tripolyphosphate.
3 products
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.
NHTSA•MODERATEEmber Overland, E-Series, Touring Series Travel TrailersEmber recalls 2027 Overland, E-Series, and Touring trailers over incorrect VIN on certification label.
FDA•LOWLidolog KitLidolog Kit is being recalled because the label wrap obscures the barcode, making it difficult to scan.
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.
NHTSA•MODERATEFord Bronco Engine Compartment Wiring HarnessFord recalls 2021-2026 Bronco and Bronco Raptor over wiring harness short circuit fire risk.
NHTSA•MODERATEBlue Bird Vision Brake LineBlue Bird recalls 2022-2027 Vision buses over brake line damage that may cause fluid leak, fire, or crash risk.
- NHTSA•MODERATEBlue Bird Vision Brake Line
Blue Bird recalls 2022-2027 Vision school buses over brake line damage risk from cotter pin contact.