FDA•MODERATE
Gerber Arrowroot Biscuits
Gerber Arrowroot Biscuits (5.5 oz, UPC 015000005962) recalled for potential paper/plastic contamination in arrowroot flour.
Filters
Category
Agency
Severity
All Recalls
Back to home ←
FDA•MODERATEAsteria Health Testosterone Sterile PelletsAsteria Health is recalling 100 mg testosterone pellets due to potential metal particulate contamination.
25 products
FDA•MODERATETrazodone Hydrochloride 50 mg TabletsGranules Pharmaceuticals is recalling Trazodone Hydrochloride 50 mg tablets (NDC 70010-231-01) due to foreign tablets or capsules in bottles.
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•MODERATEPhilips Azurion 7 M12 SystemPhilips is recalling Azurion 7 M12 systems due to a risk of unexpected table movement when the Reset Geometry button is pressed.
8 products
FDA•CRITICALRaaw Energy Dog Food Chicken MedleyRaaw Energy is recalling Dog Food Chicken Medley (2-lb and 5-lb tubes) due to Listeria, Salmonella, and Campylobacter contamination.
5 products
FDA•MODERATETops GOLD PicklesMangalm LLC is recalling Tops GOLD pickle products due to potential erucic acid contamination from mustard oil.
6 products
FDA•CRITICALNavitas Organics Organic Chia SeedsNavitas Organics is recalling 8 oz packages of Organic Chia Seeds due to potential Salmonella contamination.
FDA•MODERATEI.T.S. Headless Compression Screw SystemI.T.S. is recalling its Headless Compression Screw System due to updated MRI safety testing showing higher temperature risks.
24 products
FDA•MODERATEDatascope CS300 IABPDatascope is updating the IFU for CS300 IABP software version C.01 to correct battery runtime and cycle specifications.
2 products
FDA•MODERATERed Button Movie House PopcornLee's Commissary is recalling Red Button Movie House Popcorn due to potential foreign material contamination.
FDA•MODERATEBisoprolol Fumarate and Hydrochlorothiazide Tablets 2.5 mg/6.25 mgUnichem Pharmaceuticals recalls Bisoprolol/Hydrochlorothiazide 2.5/6.25 mg tablets (NDC 29300-187-01) due to N-Nitroso Bisoprolol impurity specification failure.
FDA•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•MODERATEAuris Health MONARCH Platform Bronchoscopy SystemAuris Health is recalling MONARCH Platform Bronchoscopy systems due to a software issue that may cause unexpected robotic arm repositioning and contact with the patient.
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•MODERATEPhysio-Control Infant/Child Defibrillator ElectrodesPhysio-Control is recalling infant/child defibrillator electrodes due to a risk of delamination that may prevent proper therapy delivery.
2 products
FDA•MODERATEMOLLI 2 Surgical Marker SystemStryker is updating the MOLLI 2 System labeling due to the risk of magnetized surgical tools dislodging markers during tissue removal.
2 products
FDA•MODERATEAdapt Pump Model 61600200Agiliti is recalling Adapt Pump Model 61600200 due to Microclimate Management function failure after Autofirm use.
FDA•MODERATECrunchy Caramel Dark ChocolateGarcia Nevett is recalling Crunchy Caramel dark chocolate bars due to an undeclared milk allergen.
FDA•MODERATEMed Nap BZK Antiseptic TowelettesAcme United is recalling Med Nap BZK Antiseptic Towelettes (NDC 0924-0246-01) due to CGMP deviations.
22 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•MODERATECobas Pro Integrated Solutions Analytical UnitsRoche is recalling Cobas Pro integrated solutions due to a software defect causing the system to report erroneous, repeated lab results.
2 products
FDA•MODERATEAtellica CH Urine Albumin TestSiemens is recalling Atellica CH Urine Albumin tests (Material 11537225) due to falsely depressed results in high-concentration samples.
FDA•MODERATERoasted Tomato and Parmesan Focaccia BreadBakkavor is recalling various roasted tomato and parmesan focaccia breads due to potential metal fragment contamination.
3 products
FDA•CRITICALOrganic Black Chia SeedsTradin Organics is recalling 55.12 lb bags of organic black chia seeds due to potential Salmonella contamination.
FDA•MODERATEVegetarian Chicken Flavor RamenPalmetto Gourmet Foods is recalling Vegetarian Chicken Flavor Ramen due to undeclared Yellow #5.
2 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•MODERATEPremium Food Jordan AlmondsPremium Food Jordan Almonds are recalled for undeclared wheat and color additives.
2 products
FDA•MODERATESimply Nature Spinach BitesDr. Praeger's is recalling Simply Nature Spinach Bites (12 oz) due to possible rodent hair contamination.
FDA•MODERATEWoodland Gourmet Arrowroot FlourWoodland Gourmet Arrowroot Flour is being recalled due to the potential presence of foreign material.
FDA•CRITICALUDENYCA Pegfilgrastim-cbqv InjectionUDENYCA pegfilgrastim-cbqv prefilled syringes (Lot 2199821) recalled due to improper storage temperature.
FDA•MODERATEThyroid, USPSpecialty Process Labs is recalling Thyroid, USP (NDC 81305-100-02) due to subpotency.
FDA•MODERATEMediHoney Gel DressingIntegra LifeSciences is recalling MediHoney Gel dressings (catalog numbers 31805 and 31815) due to a potential sterile barrier breach.
3 products
FDA•CRITICALOlympus High Flow Insufflation UnitOlympus is recalling the High Flow Insufflation Unit, Model UHI-3, due to a software issue that may lead to overpressure events.
3 products
FDA•MODERATEGE Healthcare Centricity Universal Viewer Zero Footprint ClientGE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client (Models 2110344-039, -046, -047) due to patient information and image mismatch risk.
FDA•MODERATEAonic Complete Hers Dietary SupplementAonic Complete Hers dietary supplement shots are recalled due to potential E. coli, coliform, and Pseudomonas aeruginosa contamination.
2 products
FDA•CRITICALLive it Up Super Greens Dietary SupplementLive it Up Super Greens dietary supplement is recalled due to potential Salmonella Typhimurium contamination.
4 products
FDA•LOWLubna Quality Products Mung BeansLubna Quality Products is recalling 4 lb mung bean packages due to unapproved pesticide (Thiamethoxam) contamination.
FDA•MODERATEWinCo Foods Deli Margherita PizzaWinCo Foods is recalling Deli Margherita Pizza Thin Crust due to potential metal fragment contamination.
FDA•MODERATEMethylprednisolone Tablets USP Dosepak 4 mgGreenstone is recalling methylprednisolone 4 mg tablets (NDC 59762-4440-2) due to incorrect blister foil orientation causing incorrect dosing information.
FDA•MODERATEReverse Shoulder Prosthesis Humeral Socket InsertEncore Medical is recalling the RSP Humeral Socket Insert (model 509-00-432) due to incorrect product labeling.
3 products
FDA•MODERATEAesculap Minop TrocarAesculap is recalling the Minop Trocar 150mm (Model FF399R) due to a potential defect where the trocar shaft length may be too long.
FDA•MODERATEMedline Unna-Z Stretch Zinc Paste BandageMedline is recalling Unna-Z Stretch Zinc Paste Bandages due to a labeling error omitting castor oil and calamine ingredients.
FDA•MODERATEMargarita Thin Crust PizzaRose and Shore is recalling Margarita Thin Crust Pizzas due to potential metal contamination in the tomato ingredient.
FDA•MODERATESpicely Organic Garlic SaltSpicely Organic Garlic Salt is recalled due to undeclared salt in the product.
3 products
FDA•MODERATESevillo Fine Foods Slow Roasted Diced TomatoesSevillo Fine Foods is recalling 24 lb bulk boxes of frozen Slow Roasted Diced Tomatoes due to potential metal fragment contamination.
2 products
FDA•MODERATEOxycodone Hydrochloride Tablets, USP 5 mgAmerican Health Packaging is recalling Oxycodone Hydrochloride 5 mg tablets due to defective blister card seals that allow tablets to fall out.
FDA•MODERATEPIE PAK Trolley SystemEdermy is recalling PIE PAK trolley systems (models P2HC-A, P2HC-S, P2HC) due to a lack of required 510(k) clearance.
2 products
FDA•MODERATESpicy Breakfast BurritoMG Foods is recalling 10 oz Spicy Breakfast Burritos due to potential contamination with small hard plastic fragments.
FDA•LOWSodexo Stars Saccharin Pink PacketsSodexo Stars Saccharin (Pink) packets are recalled due to undeclared aspartame, which may pose a risk to individuals with PKU.