FDA•MODERATE
Tornier HRS Max Tuberosity Body and Trial Parts
Tornier is recalling shoulder system components incorrectly labeled as HRS Max parts, as they are incompatible with the HRS Max system.
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FDA•MODERATEMedline Anterior Hip Pack Biopsy ValveMedline is recalling Anterior Hip Packs containing Olympus biopsy valves over risk of rubber fragment detachment.
8 products
FDA•MODERATESIGNA Premier MR Scanner Magnet FittingsGE Healthcare is recalling SIGNA Premier MR scanners due to ferrous magnet fittings that could cause personnel injury during service.
FDA•MODERATEMedtronic MiniMed Insulin PumpsMedtronic MiniMed recalls all Paradigm, 600, and BLE 700 series insulin pumps over insulin delivery errors that can cause severe hypoglycemia or ketoacidosis.
14 products
FDA•MODERATEBurlington Medical Wrap ApronsBurlington Medical wrap aprons may lose shielding effectiveness over time.
13 products
FDA•MODERATEOXOID Microbact 12L Listeria Identification KitOxoid is recalling Microbact 12L Listeria Kit (MB1128A, Lot 4494873) due to risk of incorrect organism identification from ambiguous color reactions.
- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo O2 Ventilator
Philips Respironics recalls Trilogy Evo O2 ventilators (SW 1.05.15.00) over delayed obstruction alarm.
4 products 
FDA•MODERATECardinal Health Monoject Tuberculin Syringe 1 mLCardinal Health is recalling Monoject Tuberculin Syringes (Catalog 1180100777) that contain U-100 insulin syringes instead, risking dosing errors.
FDA•LOWSuper World Trading: 3 Heshan Mei Heong Yuen Food Pte NiesMei Heong Yuen roasted peanuts recalled over banned cyclamate sweetener.
3 products
FDA•MODERATEMeclizine Hydrochloride Tablets 12.5 mgAmerican Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls CentrosFLO Hemodialysis Catheters over sheath introducer defect that may cause hemorrhage and other serious complications.
5 products
FDA•MODERATEPrazosin Hydrochloride Capsules 1mgAppco Pharma recalls Prazosin HCl 1mg capsules over nitrosamine impurity (NNP) above acceptable limits.
3 products
FDA•MODERATEK.C. Pharmaceuticals: Multiple Eye DropsK.C. Pharmaceuticals recalls multiple brands of sterile eye drops over sterility concerns.
15 products
FDA•MODERATEJFE FRANCHISING: 7 productsJFE recalls Dumpling Party Trays and Loaded Dumpling Vegetable products over possible glass contamination.
7 products
FDA•MODERATETramadol Hydrochloride Tablets 50 mgAmneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.
FDA•MODERATECurosurf (poractant alfa) 240 mg Intratracheal SuspensionChiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.
FDA•MODERATESynthes VOLT Locking Screw TapSynthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.
2 products
FDA•MODERATEOlympus SOLTIVE Laser SystemOlympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
FDA•MODERATEVital Nutrients Aller-CVital Nutrients Aller-C is recalled due to undeclared egg, soy, and hazelnut allergens.
FDA•MODERATEOctreotide Acetate Injectable Suspension 20 mgTeva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.
6 products
FDA•MODERATEArtoura Breast Tissue ExpandersA recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.
7 products
FDA•MODERATEPhilips Allura Xper FD10/FD20 Wired Foot SwitchPhilips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.
22 products
FDA•MODERATEMedline ENFit G-Tube ConnectorMedline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.
2 products
FDA•MODERATEJiffy Original Composite Polisher Cups (Coarse)Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.
FDA•MODERATESterile Radiology Procedure Kits Model DYNDH1491BMedline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.
FDA•MODERATEStryker CHROMOPHARE Softlit Ring Surgical LightStryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential ceiling cover support failure.
FDA•MODERATEParadise Ultrasound Renal Denervation CatheterReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were intended to be scrapped.
3 products
FDA•MODERATEVue Motion V12 Imaging SystemPhilips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.
FDA•MODERATEPuracol and Puracol Plus Collagen Wound DressingsMedline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.
FDA•MODERATEAtellica CH Enzymatic Hemoglobin A1c AssaySiemens is recalling the Atellica CH A1c_E assay due to a risk of depressed results when used alongside the RCRP assay on the same analyzer.
FDA•MODERATEAmerican Laboratories: 3 productsAmerican Laboratories recalls pepsin powders (Full Strength, 1:10,000, 1:3000) due to potential Salmonella contamination.
3 products- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo Ventilator
Philips Respironics recalls Trilogy Evo ventilators over tidal volume discrepancy with non-pneumatic nebulizers.
4 products 
FDA•MODERATEBD Alaris System with Guardrails Suite MXBD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.
FSIS•MODERATEBlackwing Organic Meats Beef and Pork ProductsFSIS alert: Blackwing Organic Meats beef and pork products made without inspection may contain undeclared allergens or bacteria.
8 products
FDA•MODERATEBrimonidine Tartrate/Timolol Maleate Ophthalmic SolutionApotex is recalling Brimonidine Tartrate/Timolol Maleate eye drops (NDC 60505-0589-1) due to lack of sterility assurance.
FDA•MODERATEOlympus PKS Cutting ForcepsOlympus recalls PKS Cutting Forceps over jaw breakage risk from defective welds.
7 products
FDA•MODERATEMICS3 Angled Sagittal Saw AttachmentHowmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment due to a risk of external screws loosening and detaching during use.
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagsAmneal recalls Magnesium Sulfate IV bags due to product mix-up with Tranexamic Acid.
FDA•MODERATEMangalm: 6 Product Of India OilsMangalm recalls Tops GOLD pickles (6 varieties) over erucic acid risk.
6 products
FDA•MODERATELevothyroxine Sodium Tablets USP 150 mcgMacleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
FDA•MODERATELantern Knee System Drill PlateThe Lantern Knee System drill plate is recalled due to a manufacturing error that may cause excessive bone cuts during surgery.
2 products
FDA•MODERATEMiniMed 780G Insulin PumpMedtronic is recalling MiniMed 780G insulin pumps (models MMT-1884, MMT-1886) over software defects that may cause inaccurate insulin delivery.
FDA•MODERATEStraumann Custom Abutment TiStraumann recalls Custom Abutment Ti for Straumann RC due to material mix-up.
2 products
FDA•MODERATETECNIS Eyhance IOL with Simplicity Delivery SystemAMO is recalling TECNIS Eyhance IOLs with Simplicity Delivery System (model DIB00) because the lens may fail to unfold properly.
2 products
FDA•MODERATEBiDop 3 Pocket DopplerKoven Technology is recalling the BiDop 3 Pocket Doppler due to unauthorized fetal indication labeling.
2 products
FDA•MODERATEI.T.S. Headless Compression Screw SystemI.T.S. is recalling Headless Compression Screw System components due to updated MRI safety testing showing higher temperature risks.
24 products
FDA•CRITICALHandy Solutions Neck & Shoulders Heating PadHandy Solutions Neck & Shoulders Heating Pad (Model 25607) may overheat and cause burns if folded or placed under the body.
FDA•MODERATEAjinomoto Foods North America: 11 productsAjinomoto recalls frozen fried rice and gyoza dumplings over possible glass contamination.
11 products
FDA•MODERATEChilli Spanish Peanuts: 2 productsWestern Mixers recalls Chilli Spanish Peanuts (First Street 11 oz, Treasured Harvest 25 lb) due to possible glass contamination.
2 products
FDA•LOWSodium Iodide I-131 Kit Gelatin Capsule PackRadnostix is recalling Sodium Iodide I-131 Kit capsule packs due to failed product specifications.