Recalls distributed in Indiana – page 4

• functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT… recall
  FDA July 22, 2026 · Nutricia North America · Class II
• GSP Neonatal GALT Kit recall
  FDA July 15, 2026 · Wallac Oy · Class II
• Geneva Product Name: Brachytherapy Applicator Product Description: The… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• Brachytherapy Applicator Product Name: Advanced Gynecological Applicator… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote… recall
  FDA July 15, 2026 · Elekta, Inc. · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · Class II
• Intracept Access Instruments, Description recall
  FDA July 15, 2026 · Boston Scientific Neuromodulation Corporation · Class II
• Aquacel Ag Surgical SP recall
  FDA July 15, 2026 · ConvaTec, Inc · Class II
• Alabama Banana Pudding Marshmallow, 4 ounce 16 pieces of individual… recall
  FDA July 15, 2026 · Wondermade LLC · Class II
• GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component recall
  FDA July 8, 2026 · W L Gore & Associates, Inc. · Class II
• 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code:… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748… recall
  FDA July 8, 2026 · Bard Access Systems, Inc. · Class II
• Covidien Shiley Disposable Decannulation Plug recall
  FDA July 8, 2026 · Covidien, LP · Class II
• ARTIS icono ceiling recall
  FDA July 8, 2026 · Siemens Medical Solutions USA, Inc · Class II
• Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model recall
  FDA July 8, 2026 · Medela Inc · Class II
• Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton)… recall
  FDA July 8, 2026 · Teleflex LLC · Class II
• Short Monobloc Stem Broaches, Size recall
  FDA July 8, 2026 · Medacta Usa Inc · Class II
• Breathing circuit set, coaxial recall
  FDA July 8, 2026 · Hamilton Medical AG · Class I
• MorningStar Farms Hot & Spicy Sausage Patties… recall
  FDA July 8, 2026 · Mars Snacking · Class II
• MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan… recall
  FDA July 8, 2026 · Mars Snacking · Class II
• Philips Telemetry Monitor 5500 1.4 GHz recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Medium, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Medium, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 5.4 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 40 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 4.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Long, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Short, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• Surgify Halo, 3.0 mm, Extendable, Model recall
  FDA July 1, 2026 · Surgify Medical Oy · Class II
• INZONE DETACHMENT SYSTEM recall
  FDA July 1, 2026 · Stryker Neurovascular · Class II
• Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Da Vinci ASSY, PSS, SP1098, Part Number: 380601 recall
  FDA July 1, 2026 · Intuitive Surgical, Inc. · Class II
• 25# Sunflower Seeds C/S recall
  FDA July 1, 2026 · George J Howe Company, Inc. · Class I
• 5# Sunflower Seeds C/NS recall
  FDA July 1, 2026 · George J Howe Company, Inc. · Class I
• 5# Sunflower Seeds C/S recall
  FDA July 1, 2026 · George J Howe Company, Inc. · Class I