Recalls distributed in Pennsylvania – page 12

• Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
  FDA February 25, 2026 · Pure Solutions, Inc. · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, Inc. · Class II
• Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system… recall
  FDA February 18, 2026 · Elekta, Inc. · Class II
• Spectral CT 7500 on Rails recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• IQon Spectral CT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• Brilliance iCT recall
  FDA February 18, 2026 · Philips North America Llc · Class II
• CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/STRAWBERRY JAM NET WT 1 OZ (28g)… recall
  FDA February 18, 2026 · Ventura Foods LLC · Class II
• CREAMY PEANUT BUTTER NET WT 1.12 OZ(32g)/GRAPE JELLY NET WT 1 OZ (28g)… recall
  FDA February 18, 2026 · Ventura Foods LLC · Class II
• CREAMY PEANUT BUTTER NET WT 0.75 OZ(21g) DISTRIBUTED BY US FOODS… recall
  FDA February 18, 2026 · Ventura Foods LLC · Class II
• Sonic Tots, item number SON00543. Frozen potato product is packaged in… recall
  FDA February 18, 2026 · McCain Foods USA Inc · Class II
• Ore-Ida Tater Tots shaped potatoes, item number OIF00215A… recall
  FDA February 18, 2026 · McCain Foods USA Inc · Class II
• Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel… recall
  FDA February 18, 2026 · Costco Wholesale Corporation · Class I
• Molift Product Name: Molift 4-point sling bars (Accessory to mobile… recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift 2-point sling bars (Accessory to mobile… recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift Mover 300 Model recall
  FDA February 11, 2026 · Etac A/S · Class II
• Molift Product Name: Molift Mover 205 Model recall
  FDA February 11, 2026 · Etac A/S · Class II
• Lumipulse ¿-Amyloid Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse pTau 217 Plasma Controls Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Calibrators Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model recall
  FDA February 11, 2026 · Fujirebio Diagnostics, Inc. · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Product Name: Disposable Triple… recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Disposable Triple Lumen Sphincterotome Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Single Use Sphincterotome V (Distal Wire guided) Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model recall
  FDA February 11, 2026 · Olympus Corporation of the Americas · Class II
• Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical 25GA Backflush, VS0270.25 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical TID Pharos Illuminated Depressor, VS0801B recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Vortex Surgical I2 Injection Kit, VS0500 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II
• Tecfen Retractable Membrane Polisher, QTPR1267-23 recall
  FDA February 11, 2026 · Vortex Surgical Inc. · Class II