Recalls distributed in Rhode Island – page 9

• Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner +… recall
  FDA August 20, 2025 · Carefree Surgical Specialties · Class II
• Clover Valley Instant Coffee, NET WT 8 OZ (227 g)… recall
  FDA August 20, 2025 · Dollar General Corporation · Class II
• BD Alaris Pump Infusion Sets recall
  FDA August 13, 2025 · CareFusion 303, Inc. · Class I
• BD Alaris Pump Module Model, 8100 with Guardrails… recall
  FDA August 13, 2025 · CareFusion 303, Inc. · Class I
• Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt 13.5 oz (383g) recall
  FDA August 13, 2025 · Give And Go Prepared Foods Corp · Class II
• Volcano Visions Digital IVUS Catheter: PV.014P (Platinum) recall
  FDA August 6, 2025 · Volcano Corp · Class II
• HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The… recall
  FDA August 6, 2025 · HeartSine Technologies Ltd · Class II
• Stryker, StrykeFlow recall
  FDA July 30, 2025 · Stryker Corporation · Class II
• Stryker, StrykeFlow recall
  FDA July 30, 2025 · Stryker Corporation · Class II
• Covidien Nellcor Bedside SpO2 Patient Monitoring System recall
  FDA July 30, 2025 · Covidien, LP · Class II
• Natus Brain Monitor Breakout Box, Part Number 021911 recall
  FDA July 30, 2025 · Excel Tech. · 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
• Ritz Peanut Butter Cracker Sandwiches, Net Wt recall
  FDA July 30, 2025 · Mondelez Global Llc · Class II
• Ritz Cracker Sandwiches, Variety 20 count variety Pack… recall
  FDA July 30, 2025 · Mondelez Global Llc · Class II
• Ritz Peanut Butter Cracker Sandwiches, Net Wt recall
  FDA July 30, 2025 · Mondelez Global Llc · Class II
• Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz… recall
  FDA July 30, 2025 · Mondelez Global 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
• 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
• ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW… recall
  FDA July 2, 2025 · Encore Medical, LP · Class II
• ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW… recall
  FDA July 2, 2025 · Encore Medical, LP · Class II
• ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW… recall
  FDA July 2, 2025 · Encore Medical, LP · Class II
• ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW… recall
  FDA July 2, 2025 · Encore Medical, LP · Class II
• MIGHTYLICIOUS Vegan Oatmeal Coconut Cookies Gluten-Free, Dairy-Free… recall
  FDA July 2, 2025 · Mightylicious Inc. · Class I
• FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT… recall
  FDA July 2, 2025 · Firehook · Class II
• Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment recall
  FDA June 25, 2025 · Preat Corp · Class II
• iBOT PMD with software version 01.05.24. Personal Mobility Device recall
  FDA June 18, 2025 · Mobius Mobility LLC · 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
• 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
• AMCE GREEK SALAD AUTHENTIC FS, Refrigerated… recall
  FDA June 11, 2025 · Albertsons Companies LLC · Class I
• 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
• 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
• Bard¿ Single Intragastric Linton Balloon Tube recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard Blakemore Esophageal-Nasogastric Tube (Adult) recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I
• Bard Minnesota Four Lumen Esophagogastric Tamponade Tube recall
  FDA May 28, 2025 · C.R. Bard Inc · Class I