Recalls distributed in Illinois – page 5

• Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS recall
  FDA July 22, 2026 · Orthofix U.S. LLC · Class II
• Orthofix MINIRAIL, SHORT, LENGTHENER recall
  FDA July 22, 2026 · Orthofix U.S. LLC · Class II
• Orthofix MINIRAIL, STANDARD LENGTHENER Model recall
  FDA July 22, 2026 · Orthofix U.S. LLC · 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
• ABIOMED Intro Kit, 14Fr x 13 and 25 cm, PKGD, JP… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Set, Pump Set Code 0048-0044 recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Set, Pump Set Code 0048-0014 recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella 5.5 SmartAssist S2 Set, JP, Pump Set Codes 1000459, 1000460 recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella 5.5 Smart Assist Set, JP, Pump Set Codes 1000211, 1000212 recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Introducer Kit 14 Fr, 25 cm, Pump Set Code 0052-0039… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Code 0052-0038… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Introducer Kit 23 Fr, 11 cm, Pump Set Code 1000441… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Introducer Kit 14 Fr, 13 and 25 cm… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella CP Set, Pump Set Code 0048-0003… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• ABIOMED Impella RP Flex with SmartAssist Set, Pump Set Code 1000323… recall
  FDA July 22, 2026 · Abiomed, Inc. · Class I
• Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ… recall
  FDA July 22, 2026 · Amy's Kitchen 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
• GSP Neonatal GALT Kit recall
  FDA July 15, 2026 · Wallac Oy · 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
• 5008X Blood Tubing Set, 24 units per case recall
  FDA July 15, 2026 · Fresenius Medical Care Holdings, Inc. · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · Class II
• EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model recall
  FDA July 15, 2026 · Encore Medical, LP · 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
• MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites recall
  FDA July 8, 2026 · Bd Switzerland Sarl · Class II
• Covidien Shiley Disposable Decannulation Plug recall
  FDA July 8, 2026 · Covidien, LP · Class II
• Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model recall
  FDA July 8, 2026 · Medela Inc · Class II
• Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton)… recall
  FDA July 8, 2026 · Teleflex LLC · Class II
• IntelliCuff, Portable automatic cuff pressure controller recall
  FDA July 8, 2026 · Hamilton Medical AG · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CV… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters KIT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT… recall
  FDA July 8, 2026 · Medline Industries, LP · Class II
• Breathing circuit set, coaxial recall
  FDA July 8, 2026 · Hamilton Medical AG · Class I
• MorningStar Farms Hot & Spicy Sausage Patties… recall
  FDA July 8, 2026 · Mars Snacking · Class II
• MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan… recall
  FDA July 8, 2026 · Mars Snacking · Class II