Recalls distributed in Delaware – page 2

• 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
• DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L) recall
  FDA August 5, 2026 · Galliker Dairy Co, 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
• 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
• TMINI Femur Tracking Array recall
  FDA July 15, 2026 · Think Surgical, 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
• 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
• Breathing circuit set, coaxial recall
  FDA July 8, 2026 · Hamilton Medical AG · Class I
• INZONE DETACHMENT SYSTEM recall
  FDA July 1, 2026 · Stryker Neurovascular · Class II
• Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A recall
  FDA July 1, 2026 · Philips North America Llc · Class II
• HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• HeartMate Product Name: HeartMate 3" System Controller Model recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits… recall
  FDA June 24, 2026 · Thoratec LLC · Class II
• iLet Bionic Pancreas recall
  FDA June 24, 2026 · Beta Bionics, Inc. · Class II
• Mito Red Light, Super Mobile recall
  FDA June 24, 2026 · Mito Red Light Inc · Class II
• TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16 recall
  FDA June 24, 2026 · Smith & Nephew, Inc. · Class II
• REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PICC ACCESS TRAY/ASK-04001-CG1 recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: ACCESS TRAY/ASK-04001-MC3 recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: SPINAL ANESTHESIA KIT/ASA-24090-SB; SPINAL ANESTHESIA… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PARACENTESIS KIT/ASK-00376-JHH recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I
• REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X… recall
  FDA June 24, 2026 · Arrow International, LLC · Class I