Recalls distributed in Oklahoma – page 3

• PEAK LETTUCE SHRED 1/8" 4/5# Iceberg only products recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• MARKON LETTUCE CHOP 4/5# MARKON LETTUCE SHRED 1/4" 4/5# MARKON LETTUCE… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• MARKETSIDE ICEBERG SALAD 10/24 oz recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• Cross Valley Farms LETTUCE CHOP 4/5# Cross Valley Farms LETTUCE SHRED 1/4"… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• Aquafaba Powder, Vegan Replacement, NET WT… recall
  FDA August 19, 2026 · 529 Commerce, LLC · Class I
• Grade A White In-shell Chicken eggs packaged in the following… recall
  FDA August 19, 2026 · Midwest Poultry Servc C/O H & Lelectric · Class I
• Grade A Brown In-shell Chicken eggs packaged in the following… recall
  FDA August 19, 2026 · Midwest Poultry Servc C/O H & Lelectric · Class I
• REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the… recall
  FDA August 12, 2026 · Beckman Coulter, Inc. · Class II
• REF # D23352, MicroScan LabPro V5.03 Panel Update 11 (US)… recall
  FDA August 12, 2026 · Beckman Coulter, Inc. · Class II
• Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN… recall
  FDA August 12, 2026 · Siemens Healthcare Diagnostics, Inc. · Class III
• Quantum Rehab Product Name: Quantum Rival Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: 4Front Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 4Front 2HD Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 4 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 3 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 2.0 (ilevel) Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 1450 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum rehab Product Name: Q6 Edge 2.0 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge HD Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: R-TRAK Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Q6 Edge 3 Stretto Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum Outback Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• Quantum Rehab Product Name: Quantum 4Front 2 Model recall
  FDA August 12, 2026 · Pride Mobility Products Corp. · Class II
• KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055… recall
  FDA August 12, 2026 · Kerry, Inc · Class I
• Vanderhall North America Recalls Brawley GTS Electric Recreational Off Highway Vehicles (ROVs) Due to Risk of Serious Injury or Death from…
  CPSC August 6, 2026 · Vanderhall North America
• M5 Corpus Power Wheelchair recall
  FDA August 5, 2026 · Permobil Inc · Class II
• Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock recall
  FDA August 5, 2026 · Permobil Inc · Class II
• Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that… recall
  FDA August 5, 2026 · ResMed Ltd. · Class I
• MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) recall
  FDA July 29, 2026 · Medtronic MiniMed, Inc. · Class II
• Boston Scientific TheraSphere 360 Y-90 Management Platform… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• Penumbra System RED 68 Reperfusion Catheter recall
  FDA July 29, 2026 · Penumbra, Inc. · Class II
• Ventriculostomy Kit recall
  FDA July 29, 2026 · Medtronic Neurosurgery · Class II
• SeaSpine Polyaxial Head recall
  FDA July 29, 2026 · Seaspine Orthopedics Corporation · Class II
• Power F2 Powered Fastening System, Product No recall
  FDA July 29, 2026 · Ferno-Washington Inc · Class II
• da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13… recall
  FDA July 22, 2026 · Intuitive Surgical, Inc. · Class II
• Pillsbury Bread Rolls, Kaiser Roll Dough recall
  FDA July 22, 2026 · General Mills James Ford Bell Technical Center · Class II
• Pillsbury Bread Rolls, Hard Roll Dough recall
  FDA July 22, 2026 · General Mills James Ford Bell Technical Center · Class II
• functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT… recall
  FDA July 22, 2026 · Nutricia North America · Class II
• functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT… recall
  FDA July 22, 2026 · Nutricia North America · 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
• Intracept Access Instruments, Description recall
  FDA July 15, 2026 · Boston Scientific Neuromodulation Corporation · Class II
• Radius VSM Disposable NIBP Cuff recall
  FDA July 8, 2026 · Masimo Corporation · Class II
• Radius VSM ECG pre-connected Set recall
  FDA July 8, 2026 · Masimo Corporation · 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