Nationwide recalls – page 51

• FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… recall
  FDA December 17, 2025 · Orthofix U.S. LLC · Class III
• Access 2 Reaction Vessels, individual, disposable… recall
  FDA December 17, 2025 · Beckman Coulter, Inc. · Class II
• Safe-T-Centesis 6 Fr Catheter Drainage Tray recall
  FDA December 17, 2025 · Bard Peripheral Vascular Inc · Class II
• MEDLINE PERFUSION SYRINGE recall
  FDA December 17, 2025 · Medline Industries, LP · Class II
• 1. ByHeart Whole Nutrition Infant Formula cans 24 OZ 680 grams recall
  FDA December 17, 2025 · ByHeart, INC. · Class I
• Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only… recall
  FDA December 17, 2025 · Lupin Pharmaceuticals Inc. · Class II
• Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only… recall
  FDA December 17, 2025 · Cipla USA, Inc. · Class II
• Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only… recall
  FDA December 17, 2025 · Cipla USA, Inc. · Class II
• Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only… recall
  FDA December 17, 2025 · Cipla USA, Inc. · Class II
• Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL… recall
  FDA December 17, 2025 · Winder Laboratories, LLC · Class III
• Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only… recall
  FDA December 17, 2025 · Glenmark Pharmaceuticals Inc., USA · Class III
• Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical… recall
  FDA December 17, 2025 · Fagron Compounding Services · Class II
• Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr recall
  FDA December 17, 2025 · Dr. Reddy's Laboratories, Inc. · Class III
• Lanthanum Carbonate chewable tablets, 1000mg*… recall
  FDA December 17, 2025 · Cipla USA, Inc. · Class II
• Lanthanum Carbonate chewable tablets, 1000mg*… recall
  FDA December 17, 2025 · Cipla USA, Inc. · Class II
• TREK Recalls Electric Bicycles Due to Fall or Crash Hazard
  CPSC December 11, 2025 · Trek
• Reagent Kits/ containing flow cells, components of NextSeq 550Dx… recall
  FDA December 10, 2025 · Illumina, Inc. · Class II
• Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
  FDA December 10, 2025 · Philips Ultrasound, Inc · Class II
• CT 5300; Software Version Number: 4.5, 5.0, 5.1 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• Incisive CT recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• Hemochron Activated Clotting Time Low-Range Test Cuvette recall
  FDA December 10, 2025 · Accriva Diagnostics, Inc. · Class II
• MAMMOMAT Fusion recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• MAMMOMAT Inspiration recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• MAMMOMAT Revelation recall
  FDA December 10, 2025 · Siemens Medical Solutions USA, Inc · Class II
• Olympus OER-Mini recall
  FDA December 10, 2025 · Aizu Olympus Co., Ltd. · Class II
• Olympus OER-Pro recall
  FDA December 10, 2025 · Aizu Olympus Co., Ltd. · Class II
• Olympus OER-Elite recall
  FDA December 10, 2025 · Aizu Olympus Co., Ltd. · Class II
• Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail recall
  FDA December 10, 2025 · Paragon 28, Inc. · Class II
• IntelliVue Patient Monitor MX850. Product Number: 866470 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX800. Product Number: 865240 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX750. Product Number: 866471 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX700. Product Number: 865241 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX600. Product Number: 865242 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX550. Product Number: 866066 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX500. Product Number: 866064 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX450. Product Number: 866062 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX400. Product Number: 866060 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Patient Monitor MX100. Product Number: 867033 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Multi-Measurement Module X3. Product Number: 867030 recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue Multi Measurement Server X2. Product Number: M3002A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP90. Product Number: M8010A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP80. Product Number: M8008A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP70. Product Number: M8007A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP60. Product Number: M8005A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP50. Product Number: M8004A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP40. Product Number: M8003A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP30. Product Number: M8002A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP20. Product Number: M8001A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP5. Product Number: M8105A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• IntelliVue MP2. Product Number: M8102A recall
  FDA December 10, 2025 · Philips North America Llc · Class II
• Ivenix Infusion System (IIS), Large Volume Pump recall
  FDA December 10, 2025 · Fresenius Kabi USA, LLC · Class II
• Welch Allyn INF BAG, Thigh 1-Tube, Model recall
  FDA December 10, 2025 · Baxter Healthcare Corporation · Class II
• 8 in 1 STI Test Kit recall
  FDA December 10, 2025 · Get Tested International Ab · Class II
• 3 in 1 STI Test recall
  FDA December 10, 2025 · Get Tested International Ab · Class II
• 2 in 1 Trichomonas / Gardnerella Test recall
  FDA December 10, 2025 · Get Tested International Ab · Class II
• Serotonin Test recall
  FDA December 10, 2025 · Get Tested International Ab · Class II
• Pollen Allergy Test recall
  FDA December 10, 2025 · Get Tested International Ab · Class II