Recalls distributed in South Dakota – page 10

• Covidien Nellcor Bedside SpO2 Patient Monitoring System recall
  FDA July 30, 2025 · Covidien, LP · Class II
• Endosee System Convenience Kit with IV Tube recall
  FDA July 30, 2025 · CooperSurgical, Inc. · Class II
• Endosee System Convenience Kit recall
  FDA July 30, 2025 · CooperSurgical, Inc. · Class II
• HSG Procedure Tray recall
  FDA July 30, 2025 · CooperSurgical, Inc. · Class II
• EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS… recall
  FDA July 23, 2025 · Encore Medical, LP · Class II
• EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS… recall
  FDA July 23, 2025 · Encore Medical, LP · Class II
• SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve recall
  FDA July 23, 2025 · ICU Medical, Inc. · Class II
• Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz recall
  FDA July 23, 2025 · World Market Management Services, LLC · Class I
• Alcon Laboratories, Inc recall
  FDA July 16, 2025 · Alcon Research LLC · Class II
• Alcon Laboratories, Inc recall
  FDA July 16, 2025 · Alcon Research LLC · Class II
• Alcon Laboratories, Inc recall
  FDA July 16, 2025 · Alcon Research LLC · Class II
• 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
• 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
• Shore Lunch BREADING & BATTER MIX OVEN STYLE A savory… recall
  FDA July 2, 2025 · Homegrown Family Foods LLC · Class I
• 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
• SmartPath to dStream for 1.5T¿ recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera Achieva 1.5T Pulsar recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Omni/Stellar recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Master/Nova Product Number: 781106 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Explorer/Nova Dual Product Number: 781108 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Achieva Nova-Dual Product Number: 781173 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Achieva Nova Product Number: 781172 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Intera 1.5T Achieva IT Nova Product Number: 781175 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Achieva XR Product Numbers: (1) 781153, (2) 781253 recall
  FDA June 18, 2025 · Philips North America Llc · Class II
• Newport HT70 Ventilator recall
  FDA June 18, 2025 · Covidien, LP · Class I
• 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
• 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
• Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72… recall
  FDA June 4, 2025 · Ultra Clean Systems, Inc. · Class II
• Bard¿ Single Intragastric Linton Balloon Tube recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I