Recalls distributed in Maryland – page 10

• Equinoxe Product Name: Equinoxe Core Instrument Kit Model recall
  FDA March 18, 2026 · Exactech, Inc. · Class II
• Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model recall
  FDA March 18, 2026 · Exactech, Inc. · Class II
• Gelsoft Plus recall
  FDA March 11, 2026 · Vascutek, Ltd. · Class II
• AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model recall
  FDA March 11, 2026 · Aesculap Inc · Class II
• MRI LED Mobile Exam Light Battery recall
  FDA March 4, 2026 · MRIMed Inc. · Class II
• Wellsley Farms Farm- Raised Atlantic Salmon Net WT. 32 oz recall
  FDA March 4, 2026 · Slade Gorton & CO., Inc. · Class II
• NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS:… recall
  FDA March 4, 2026 · Navitas, LLC. · Class I
• Yoyo Gummy Grape Plus Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
  FDA March 4, 2026 · Sb Food LLC · Class II
• Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
  FDA March 4, 2026 · Sb Food LLC · Class II
• Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case recall
  FDA March 4, 2026 · Sb Food LLC · Class II
• Prime Food Processing Dried Croaker Fish recall
  FDA March 4, 2026 · Prime Food Processing 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
• 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
• 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
• MiniMed 780G Insulin Pump recall
  FDA February 11, 2026 · Medtronic MiniMed, Inc. · Class II
• Da Vinci Product Name: da Vinci X, Xi Surgical System… recall
  FDA February 11, 2026 · Intuitive Surgical, Inc. · Class II