FDA•MODERATE
Semaglutide Injection 2 mg Multi-Dose Vials
New Life Pharma recalls semaglutide 2 mg vials over sterility concerns.
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FDA•MODERATEAmnesteem Isotretinoin Capsules 40 mgMylan is recalling Amnesteem Isotretinoin 40 mg capsules (NDC 0378-6614-93) due to failed dissolution specifications.
FDA•MODERATESodium Iodide (I-131) Therapeutic Oral SolutionRadnostix is recalling Sodium Iodide (I-131) Therapeutic Oral Solution due to the presence of particulate matter.
FDA•MODERATEArtelon FlexBand Dynamic MatrixArtelon FlexBand Dynamic Matrix recalled over failed endotoxin testing.
3 products
FDA•MODERATEBeckman Coulter DxC 700 AU Chemistry AnalyzerBeckman Coulter recalls DxC 700 AU and AU5800 analyzers over software delay risk.
2 products- Device RecallFDA•MODERATEHealthCast Vital Sync Remote Patient Monitoring System
HealthCast is recalling Vital Sync software due to a failure to transmit or receive critical patient bedside monitor alarms.
2 products 
FDA•MODERATEEndoVive Safety PEG KitBoston Scientific is recalling EndoVive Safety PEG Kits due to compromised seals on the included antiseptic swabsticks.
FDA•MODERATELowes Foods Sour Cream and Onion Potato ChipsUncle Ray's recalls Lowes Foods sour cream & onion chips (8 oz) over inaccurate nutrition and undeclared MSG.
FDA•MODERATEEndo-Model Replacement PlateauEndo-Model Replacement Plateau is recalled due to a risk of bushing detachment from the screw shaft caused by longitudinal fractures.
13 products
FDA•MODERATEGEM Premier 5000 PAKInstrumentation Laboratory is recalling GEM Premier 5000 PAK cartridges due to errors that may cause ejection and delay patient results.
20 products
FDA•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that could impact therapy delivery.
2 products
FDA•MODERATEAPTUS 2.5 TriLock ScrewsMedartis is recalling APTUS 2.5 TriLock Screws (model A-5750.16/1) due to a mix-up with 2.8mm screws.
2 products
FDA•MODERATEVegetarian Chicken Flavor RamenPalmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen 3oz packages due to undeclared Yellow #5.
2 products
FDA•MODERATEEquinoxe Core Instrument KitExactech recalls Equinoxe Core Instrument Kit and Ergo Impactor Handle over missing cross-pin risk.
2 products
FDA•LOWC2O Coconut Water with Pulp 17.5 ozC2O Coconut Water with Pulp 17.5 oz recalled over incorrect outer box labeling omitting added sugar.
FDA•MODERATERaz Mobile Shower Commode ChairsRaz Design is recalling various mobile shower commode chairs due to a seat bracket issue that may pose a fall risk to users.
2 products
FDA•MODERATEMedline Unna-Z Stretch Zinc Paste BandageMedline is recalling Unna-Z Stretch Zinc Paste Bandages due to an incomplete ingredient list on the label.
FDA•MODERATEBD 10mL Non-Sterile Luer-Lok SyringeBD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.
FDA•MODERATEIBA Proton Therapy System PROTEUS 235IBA PROTEUS 235 proton therapy systems may fail to stop beam delivery if external gating device signal is lost, risking patient mistreatment.
CPSC•Tomum Minoxidil Hair Growth TreatmentTomum Minoxidil Hair Growth Treatment is recalled because the non-child-resistant packaging poses a poisoning risk to young children.
CPSC•Cubimana Island Storm 3-in-1 Building SetsCubimana Island Storm building sets (Model HG1004) are recalled because the LED light's battery compartment poses a serious ingestion hazard.
CPSC•Forever 21 Kids Disney Mickey Mouse Pajama PantsForever 21 Kids Disney Mickey Mouse Pajama Pants are recalled for violating federal flammability standards, posing a serious burn hazard.
CPSC•HALO Magic SleepsuitsHALO is recalling Magic Sleepsuits due to a choking hazard from detachable zipper heads.
FDA•MODERATEHTO Nevada: Multiple Dermal Source ProductsKirkman recalls Vasocaine Spray and Zone 1/2 Lidocaine Creams over unsupported expiry dates.
3 products
FDA•MODERATEOlympus ShockPulse-SE Lithotripsy System GeneratorOlympus is recalling the ShockPulse-SE Lithotripsy System generator due to a wiring issue that may cause treatment delays.
2 products
FDA•Miss Vickie's Spicy Dill Pickle Potato ChipsFrito-Lay recalls Miss Vickie's Spicy Dill Pickle chips (8 oz.) over undeclared milk allergen.
FDA•MODERATEVergani Pandoro Classico Gluten FreeVergani Pandoro Classico Gluten Free recalled due to possible Teflon fragments.
FDA•MODERATEMedline Nail KitMedline is recalling the Nail Kit (model DYKM1528) because the included sterile saline wound wash may not meet sterility requirements.
5 products
FSIS•CRITICALSuzanna's Kitchen Ready-To-Eat Grilled Chicken Breast FilletsSuzanna's Kitchen recalls 13,720 lbs of ready-to-eat grilled chicken breast fillets (lot 60104 P1382 287 5 J14) over possible Listeria contamination.
FDA•MODERATEBader Enterprises: 2 Clear Flexible Plastic PackagingsBader Enterprises recalls Premium Food Jordan Almonds and Bubble Gum for undeclared wheat and FD&C Blue 1 & 2 Lake.
2 products
FDA•LOWCipla: Multiple Packaged In Cartons CapsulesCipla recalls Nilotinib 150 mg and 200 mg capsules over failed specification tests.
2 products
FDA•MODERATEMidodrine Hydrochloride Tablets, USP 5 mgMajor Pharmaceuticals is recalling Midodrine Hydrochloride Tablets 5 mg (NDC 0904-6818-06) due to inadequately sealed blister packaging.
FDA•MODERATEOlympus Single Use Biopsy ValveOlympus is recalling the MAJ-210 single use biopsy valve due to the potential for rubber fragments to detach during use.
2 products- Device RecallFDA•MODERATEDatascope CS300 IABP
Datascope is updating the Instructions for Use for the CS300 IABP (software version C.01) to correct battery runtime and cycle specifications.
2 products 
FDA•MODERATESTA Liatest Free Protein S KitDiagnostica Stago is recalling the STA Liatest Free Protein S kit due to potential underestimation of protein S levels in normal plasma.
FDA•MODERATEACME UNITED: multiple drugsAcme United is recalling 22 varieties of BZK Antiseptic Towelettes due to manufacturing process deviations.
22 products
FDA•MODERATESemaglutide Bulk APIHarbin Jixianglong recalls semaglutide bulk API over CGMP validation failures.
2 products- Device RecallFDA•MODERATEB. Braun 21G Winged Infusion Set
B. Braun recalls 21G winged infusion sets due to risk of dull or broken needle tip.
3 products 
FDA•MODERATEEVO+ Visian Toric Implantable Collamer Lens (TICL)Staar Surgical is recalling EVO+ Visian Toric ICL Model VTICM5 due to incorrect length labeling (12.1 mm labeled vs. 12.6 mm actual) causing excessive vault and potential angle closure.
FDA•MODERATEAesculap Minop TrocarAesculap is recalling the Minop Trocar 150mm because the shaft may be too long.
FDA•MODERATEAtellica CH Urine Albumin TestSiemens is recalling Atellica CH Urine Albumin tests (Material 11537225) due to falsely depressed results in high-concentration samples.
FSIS•MODERATEPunahele Jerky Beef CrispsPunahele Jerky beef crisps recalled for undeclared soy allergen; best by 2/17/2027 or prior.
4 products
FDA•MODERATESavannah Bee Honey BBQ Sauce MustardSavannah Bee Honey BBQ Sauce "Mustard" bottles may contain "Sweet" sauce with undeclared wheat and soy.
FDA•Rhino Choco VIP 10X ChocolateRhino Choco VIP 10X Chocolate recalled for undeclared Tadalafil; return for refund.
CPSC•Andersen Window Opening Control DevicesAndersen is recalling window opening control devices that can break or detach, posing fall and serious injury hazards.
CPSC•Babysense Max View Baby MonitorBabysense is recalling the Max View baby monitor (model VBM55RX) due to a fire hazard from the display unit overheating or sparking.
CPSC•Royal Oak Flame Saber LightersRoyal Oak is recalling flame saber lighters due to missing child-resistant mechanisms and safety labels, posing fire and burn hazards.
CPSC•Magnetic Chess GamesMagnetic chess games are recalled due to a magnet ingestion hazard that can cause serious injury or death to children.
CPSC•Evajoy Above-Ground PoolsEvajoy above-ground pools are being recalled due to a drowning hazard caused by a compression strap that can act as a foothold for children.
CPSC•Grtard Magnetic Stick Figure Toy SetsGrtard magnetic stick figure toy sets are recalled due to a serious magnet ingestion hazard that can cause severe injury or death in children.