Recalls distributed in New Mexico – page 2

• 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
• 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
• 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
• Pipeline Flex Embolization Device with Shield Technology… recall
  FDA July 29, 2026 · Micro Therapeutics, Inc. · Class II
• Pipeline Flex Embolization Device with Shield Technology… recall
  FDA July 29, 2026 · Micro Therapeutics, Inc. · Class II
• Power F2 Powered Fastening System, Product No recall
  FDA July 29, 2026 · Ferno-Washington Inc · Class II
• Wonton Wrappers packed into clear flexible plastic bag and sold as 40… recall
  FDA July 29, 2026 · Man Fon, Inc. · Class II
• Man Fon Inc recall
  FDA July 29, 2026 · Man Fon, 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
• 5008X Blood Tubing Set, 24 units per case recall
  FDA July 15, 2026 · Fresenius Medical Care Holdings, Inc. · Class II
• Intracept Access Instruments, Description recall
  FDA July 15, 2026 · Boston Scientific Neuromodulation Corporation · Class II
• Aquacel Ag Surgical SP recall
  FDA July 15, 2026 · ConvaTec, Inc · Class II
• High Valley Orchard Chocolate Covered Raisins, net wt recall
  FDA July 15, 2026 · Lehi Valley Trading Company, Inc · Class I
• GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component recall
  FDA July 8, 2026 · W L Gore & Associates, Inc. · 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
• Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton)… recall
  FDA July 8, 2026 · Teleflex LLC · Class II
• Breathing circuit set, coaxial recall
  FDA July 8, 2026 · Hamilton Medical AG · Class I
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II
• Convenience kits containing select SKUs of 10mL Polycarbonate Colored… recall
  FDA July 1, 2026 · Medline Industries, LP · Class II