Recalls distributed in Oklahoma – page 15

• TrueDent Clear, TDM 100, Model No recall
  FDA July 16, 2025 · Stratasys Ltd · Class III
• FEM-FLEXII Product Name: Femoral Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• FEM-FLEX II Product Name: Femoral Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• Optisite Arterial Cannula Product Name: Optisite Arterial Cannula Model recall
  FDA July 16, 2025 · Edwards Lifesciences, LLC · Class I
• REF: 666289 , BD FACS, 7-Color Setup Beads, 25 Runs, CE, IVD… recall
  FDA July 9, 2025 · Becton, Dickinson and Company, BD Bio Sciences · Class II
• REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only… recall
  FDA July 9, 2025 · Becton, Dickinson and Company, BD Bio Sciences · Class II
• REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra recall
  FDA July 9, 2025 · C.R. Bard Inc · Class II
• BD Heyman Follower Coude Tip for following sizes: 12Fr recall
  FDA July 9, 2025 · C.R. Bard Inc · Class II
• BD Heyman Follower Straight Tip for following sizes: 10Fr recall
  FDA July 9, 2025 · C.R. Bard Inc · Class II
• Apex Knee System recall
  FDA July 9, 2025 · Corin Medical, Ltd. · Class II
• Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an… recall
  FDA July 9, 2025 · Peak Cocktails · Class II
• REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487 recall
  FDA July 2, 2025 · Beckman Coulter, Inc. · Class II
• Product Name [ recall
  FDA July 2, 2025 · CareFusion 303, Inc. · Class II
• REF: 381434 BD Insyte Autoguard Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 382544 BD Insyte Autoguard Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 381811, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 381433, BD Insyte Autoguard Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 382633, BD Insyte Autoguard BC Winged… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• REF: 381423, BD Insyte Autoguard, Shielded IV Catheter… recall
  FDA July 2, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• DxI 9000 Access Immunoassay Analyzer C11137 recall
  FDA July 2, 2025 · Beckman Coulter, Inc. · Class II
• Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311… recall
  FDA June 25, 2025 · Balt USA, LLC · Class II
• Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875… recall
  FDA June 25, 2025 · Balt USA, LLC · Class II
• BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD Texium: 3 mL recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• BD Texium Needle-Free Syringe: 3 mL recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium… recall
  FDA June 18, 2025 · Bd Switzerland Sarl · Class II
• Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution recall
  FDA June 18, 2025 · Contamac Solutions, Inc. · Class II
• Newport HT70 Ventilator recall
  FDA June 18, 2025 · Covidien, LP · Class I
• IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet… recall
  FDA June 18, 2025 · Fresenius Kabi USA, LLC · Class I
• Preconception Multi for Women 60 capsules packaged in blister packs Batch… recall
  FDA June 18, 2025 · NRC Nutrition Pty Ltd · Class II
• Sample probe sucks a sample dispensed into a tube or cup and discharges… recall
  FDA June 11, 2025 · Beckman Coulter Mishima K.K. · Class II
• Sample probe sucks a sample dispensed into a tube or cup and discharges… recall
  FDA June 11, 2025 · Beckman Coulter Mishima K.K. · Class II
• Best Taste Brand Salted Shrimp Paste Sauce recall
  FDA June 11, 2025 · Country Favor Inc. · Class III
• GNC Women's 30+ Vitapak, Carton of 30 Sachets recall
  FDA June 11, 2025 · GNC Holdings LLC · Class III
• Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gummies (120… recall
  FDA June 11, 2025 · Nordic Naturals, Inc. · Class III
• Sysco Classic chocolate pudding, 7lb #10 metal can recall
  FDA June 11, 2025 · Treehouse Foods · Class II
• VITROS Chemistry Products CRP Slides recall
  FDA June 4, 2025 · Ortho-Clinical Diagnostics, Inc. · Class II
• Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5… recall
  FDA June 4, 2025 · Cardinal Health 200, LLC · Class II
• GM Helix Acqua Implant, Article Number: 140.985 recall
  FDA June 4, 2025 · Straumann USA LLC · Class II
• GM Helix Acqua Implant, Article Number: 140.984 recall
  FDA June 4, 2025 · Straumann USA LLC · Class II
• Plus Initial Drill, Article Number: 103.170 recall
  FDA June 4, 2025 · Straumann USA LLC · Class II
• ADVIA Centaur HCY Calibrator (2 Pack) recall
  FDA June 4, 2025 · Siemens Healthcare Diagnostics, Inc. · Class II
• Atellica IM Homocysteine Calibrator (2 Pack) recall
  FDA June 4, 2025 · Siemens Healthcare Diagnostics, Inc. · Class II
• Apo B Reagent recall
  FDA June 4, 2025 · Beckman Coulter Ireland, Inc. · Class III
• BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN recall
  FDA May 28, 2025 · Becton Dickinson Infusion Therapy Systems, Inc. · Class II
• Contour Product Name: Contour Gold Eyelid Weight Model recall
  FDA May 21, 2025 · Meddev Corp · Class II
• Contour Product Name: Contour Gold Eyelid Weight Model recall
  FDA May 21, 2025 · Meddev Corp · Class II
• MedicaLyte Liquid Bicarbonate Concentrate recall
  FDA May 21, 2025 · Nipro Renal Soultions USA, Corporation · Class I