Recalls distributed in Illinois – page 12

• Campy CVA Medium 100/PK, R01272 recall
  FDA March 4, 2026 · Remel, Inc · Class II
• PIE PAK Models: P2HC-A, P2HC-S, P2HC recall
  FDA March 4, 2026 · Edermy LLC · Class II
• PIE Trolley System Model: 2005 recall
  FDA March 4, 2026 · Edermy LLC · Class II
• Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL… recall
  FDA March 4, 2026 · Encore Medical, LP · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model recall
  FDA March 4, 2026 · Encore Medical, LP · Class II
• Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT… recall
  FDA March 4, 2026 · Encore Medical, LP · Class II
• MRI LED Mobile Exam Light Battery recall
  FDA March 4, 2026 · MRIMed Inc. · Class II
• Valley Springs Steamed Distilled Water recall
  FDA March 4, 2026 · Valley Springs Artesian Gold, LLC · Class II
• Valley Springs 100% Natural Bottled Water recall
  FDA March 4, 2026 · Valley Springs Artesian Gold, LLC · Class II
• Valley Springs 100% Natural Bottled Water packaged in the following size… recall
  FDA March 4, 2026 · Valley Springs Artesian Gold, LLC · Class II
• NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS:… recall
  FDA March 4, 2026 · Navitas, LLC. · Class I
• MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer… recall
  FDA February 25, 2026 · Stryker Corporation · Class II
• MONARCH Platform, Bronchoscopy recall
  FDA February 25, 2026 · Auris Health, Inc · Class II
• Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue… recall
  FDA February 25, 2026 · Bard Peripheral Vascular Inc · Class II
• Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep… recall
  FDA February 25, 2026 · Pure Solutions, Inc. · Class II
• Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
  CPSC February 19, 2026 · Meijer
• da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000… recall
  FDA February 18, 2026 · Intuitive Surgical, Inc. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, Inc. · Class II
• ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm recall
  FDA February 18, 2026 · Alphatec Spine, 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
• Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz recall
  FDA February 18, 2026 · Domino Foods Inc · Class III
• Spicy Breakfast Burrito in a flour tortilla recall
  FDA February 18, 2026 · MG Foods-Compass Group · Class II
• Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel… recall
  FDA February 18, 2026 · Costco Wholesale Corporation · Class I
• FDR Visionary Suite recall
  FDA February 11, 2026 · FUJIFILM Healthcare Americas Corporation · 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