FDA•CRITICAL
Transvenous Pacing Electrode Tray
Argon Medical recalls Transvenous Pacing Electrode Trays over non-sterile lidocaine ampules.
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FDA•CRITICALAbiomed Impella RP Flex Introducer KitAbiomed recalls Impella RP Flex introducer kits over sheath leakage risk from manufacturing defects.
13 products
FDA•CRITICALReprocessed Electrophysiology and Ultrasound CathetersMedline is recalling reprocessed catheters due to residual particulate matter that may cause infection or embolism.
FDA•CRITICALMedtronic Harmony Delivery Catheter SystemMedtronic is recalling the Harmony Delivery Catheter System due to a manufacturing defect that may cause the distal tip to detach during use.
FDA•CRITICALDSAEK Pack-RX Surgical Convenience KitWindstone Medical recalls DSAEK Pack-RX kits due to contaminated alcohol prep pads.
4 products
FDA•CRITICALHillrom Volara Patient Circuit KitHillrom Volara circuit kits recalled over nebulizer cup leakage causing oxygen drops and ineffective treatment.
4 products
FDA•CRITICALSpring & Mulberry Date-Sweetened ChocolateSpring & Mulberry is recalling Mango Chili and Pecan Date-Sweetened Chocolate bars due to potential Salmonella contamination.
11 products
FDA•CRITICALHamilton Medical Ventilator Coaxial Breathing CircuitHamilton Medical is recalling ventilator coaxial breathing circuits due to a risk of valve membrane adhesion and inadequate ventilation.
FDA•CRITICALHigh Valley Orchard Chocolate Covered RaisinsHigh Valley Orchard Chocolate Covered Raisins are recalled due to undeclared peanuts caused by a mis-packaging error.
FDA•CRITICALAbiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CPAbiomed recalls Impella CP introducer kit over thrombus risk.
4 products
FDA•CRITICALMedline Convenience KitsMedline recalls convenience kits with recalled lidocaine and bupivacaine injections due to supplier quality issues.
5 products
FDA•CRITICALNara Organics Whole Milk Organic Infant FormulaNara Organics is recalling Whole Milk Organic Infant Formula over potential Clostridium botulinum contamination.
FDA•CRITICALParacentesis KitArrow recalls paracentesis kits over supplier drug quality issues that may cause serious injury.
51 products
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling 30+ models of Impella Controllers due to a software error that may affect left ventricular support devices.
2 products
FDA•CRITICALBeekeeper's Naturals Saline Nasal SprayBeekeeper's Naturals is recalling 1 FL OZ Saline Nasal Spray bottles due to potential microbial contamination.
2 products
FDA•CRITICALCareFusion 213: Multiple Chlorhexidine Gluconate ProductsCareFusion recalls BD ChloraPrep Clear and FREPP Clear applicators over sterility concerns from lidding wrinkles.
4 products
FDA•CRITICALDoxorubicin Hydrochloride Liposome InjectionNorthstar Rx is recalling Doxorubicin Hydrochloride Liposome injection 50 mg/25 mL vials due to potential glass particulate contamination.
FDA•CRITICALHaleon US: multiple drugsHaleon is recalling Gas-X Extra Strength softgels in 72-count and 120-count packages due to potential chemical contamination.
2 products
FDA•CRITICALThe Coffee Connexion Co: 4 productsCoffee Connexion recalls cheese sauce mixes due to potential Salmonella from supplier's dry milk powder.
4 products
FDA•CRITICALDraeger Atlan A350 Anesthesia WorkstationDraeger recalls Atlan A350 anesthesia workstation over ventilator failure risk.
2 products
FDA•CRITICALKayserBett IDA Pediatric Care BedKayserBett is recalling the IDA pediatric care bed due to an entrapment risk if the hand control is not locked while the child is unattended.
- Device RecallFDA•CRITICALIvenix Infusion System LVP Software
Fresenius Kabi is recalling Ivenix Infusion System LVP software due to a potential battery-health reporting error that may cause pump shutdown.
FDA•CRITICALDesign Options Spinal TrayB. Braun recalls Design Options Spinal Trays due to potential quality issues in bupivacaine component.
6 products
FDA•CRITICALBD Spinal Tray with Quincke NeedleBD recalls Spinal Tray with Quincke Needle (Cat. 405609) due to quality issues in bupivacaine component.
10 products
FDA•CRITICALMedline Anesthesia TraysMedline recalls anesthesia trays containing Huons bupivacaine injection over data integrity and efficacy issues.
10 products
FDA•CRITICALOmnipod 5 PodsInsulet recalls Omnipod 5 Pods over insulin leakage risk that may cause high blood glucose, DKA, or HHS.
3 products
FDA•CRITICALTNVitamins and Doctor's Pride Moringa CapsulesTotal Nutrition is recalling TNVitamins and Doctor's Pride Moringa capsules due to potential Salmonella contamination.
FDA•CRITICALMogo Pure Moringa Oleifera CapsulesMogo Moringa is recalling Pure Moringa Oleifera Capsules due to potential Salmonella Typhimurium contamination.
FDA•CRITICALAbiomed Automated Impella ControllerAbiomed is recalling the Automated Impella Controller due to hardware issues that may cause motor control, startup, or power failures.
FDA•CRITICALPS Seasoning & Spices: 6 productsPS Seasoning & Spices recalls Ellsworth Sour Cream + Onion Seasoning and five other products over possible Salmonella from recalled milk powder.
6 products
FDA•CRITICALMG217 Multi-Symptom Treatment CreamWisconsin Pharmacal is recalling MG217 Multi-Symptom Treatment Cream due to Staphylococcus aureus contamination.
FDA•CRITICALArrow Edge Hemodialysis Catheterization KitArrow recalls hemodialysis kits over sheath introducer splitting failure risk.
6 products
FDA•CRITICALMedline Namic Angiographic Control Syringe KitsWindstone Medical is recalling Medline Namic Angiographic Control Syringe kits due to a risk of adapter disconnection and potential injury.
FDA•CRITICALNamic Angiographic ManifoldMedline recalls Namic Angiographic Manifolds (SKU 64038200) over particulate in fluid path.
14 products
FDA•CRITICALJOHN B SANFILIPPO & SONS: 6 productsJohn B. Sanfilippo recalls trail mixes over possible Salmonella contamination.
6 products
FDA•CRITICALBeacon Tip Centimeter Sizing CatheterCook recalls Beacon Tip Centimeter Sizing Catheters due to risk of marker band cracking and device fragmentation.
3 products
FDA•CRITICALIntuitive SureForm 30 Gray ReloadsIntuitive is recalling SureForm 30 Gray stapler reloads due to the risk of an incomplete staple line during surgical procedures.
FDA•CRITICALLactated Ringer's Injection USPB. Braun Medical is recalling Lactated Ringer's Injection USP due to the presence of particulate matter.
FDA•CRITICALFrench Broad Chocolate Bette's Bake Sale BonbonsFrench Broad Chocolate is recalling Bette's Bake Sale bonbons due to an undeclared walnut allergen caused by mislabeled tasting guides.
FDA•CRITICALB. Braun Streamline Bloodline SetB. Braun recalls Streamline Bloodline Sets for Dialog over air bubble risk.
6 products
FDA•CRITICALBlaine Labs: multiple drugsBlaine Labs recalls Revitaderm Wound Care Gel and other products over microbial contamination.
9 products
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagAmneal is recalling Magnesium Sulfate IV bags (NDC 70121-1720-3) due to product mix-up with Tranexamic Acid.
FDA•CRITICALMedline Convenience Kits with Namic RA SyringesMedline recalls convenience kits with Namic RA syringes due to risk of loose connection or disconnection during use.
25 products- Device RecallFDA•CRITICALPhilips Respironics Trilogy Evo Ventilator
Philips Respironics recalls Trilogy Evo ventilators over delayed obstruction alarm.
4 products 
FDA•CRITICALCentrosFLO Hemodialysis CathetersMerit Medical recalls 80+ CentrosFLO hemodialysis catheter variants over sheath introducer splitting defect.
5 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•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•CRITICALErbe Flexible CryoprobeErbe recalls Flexible Cryoprobes (REF 20402-401) due to rupture/burst risk.
4 products
FDA•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
FDA•CRITICALOmnipod 5 PodsInsulet is recalling Omnipod 5 Pods due to a cannula defect that can cause insulin under-delivery and severe health risks.