Recalls distributed in Tennessee – page 3

• TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR FARMS BLEND… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• SYSCO BLEND LETT/ROM 50/50 NOCLR 4/5# SYSCO BLEND LETT/ROM 70/30 NOCOLR… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5#… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• YUM LETTUCE SHREDDED 1/4" 6/5# Iceberg only products recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• Jack in the Box 1/8" SHRED LETTUCE 4/5# Iceberg only products recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• TAYLOR FARMS LETTUCE CHOP 1X1" 4/4# TAYLOR FARMS LETTUCE CHOP 1X1" 8/2#… recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• SYSCO LETTUCE CHOP 4/5# SYSCO 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
• SUBWAY SHRED LETTUCE 1/4" 4/5# Iceberg only products recall
  FDA August 19, 2026 · Taylor Farms de Mexico S. de R.L. de C.V. · Class I
• 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
• 5-PLASMA Bivalirudin Control, Model Number 5D-44905 recall
  FDA August 12, 2026 · Aniara Diagnostica LLC · Class II
• 5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905 recall
  FDA August 12, 2026 · Aniara Diagnostica LLC · Class II
• 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905 recall
  FDA August 12, 2026 · Aniara Diagnostica LLC · Class II
• 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
• HardyDisk AST Cefiderocol 30¿g (FDC30) recall
  FDA August 12, 2026 · Hardy Diagnostics · Class II
• FilmArray NGDS Warrior Panel recall
  FDA August 12, 2026 · Biofire Defense · Class II
• 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
• Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN:… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• Radial Jaw 4 Large Capacity Biopsy Forceps with the following descriptions… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• Radial Jaw 4 Standard Capacity Biopsy Forceps with the following… recall
  FDA August 12, 2026 · Boston Scientific Corporation · Class II
• Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree… recall
  FDA August 12, 2026 · PT Organics Limited · Class II
• Spicy Breakfast Burrito sold under the following brand names: FRESH &… recall
  FDA August 12, 2026 · M.G. Foods, Inc. · Class I
• Stryker Hoffmann II Connecting Rod Micro 3 x 150mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 120mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 90mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 60mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 50mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 40mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• Stryker Hoffmann II Connecting Rod Micro 3 x 30mm recall
  FDA August 5, 2026 · Stryker GmbH · Class II
• OsteoBallast, 45 x 17.5 mm (SeaSpine Brand) recall
  FDA August 5, 2026 · IsoTis OrthoBiologics, Inc. · Class II
• M5 Corpus Power Wheelchair recall
  FDA August 5, 2026 · Permobil Inc · Class II
• L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm… recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, 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
• SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall
  FDA July 29, 2026 · Kent Imaging, 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