Recalls distributed in South Dakota

Recalls whose official distribution list names South Dakota. A further 6,837 recalls were distributed nationwide and may also affect South Dakota; see the nationwide list.

792 recalls published between October 9, 2024 and September 30, 2026 (791 FDA, 1 CPSC). Most common issues: sterility (129), injury risk (67), microbial contamination (57), software (36). 145 were FDA Class I, the most serious level.

Nationwide recalls →

• nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US… recall
  FDA September 30, 2026 · Criticare Technologies, Inc. · Class II
• ForeSight Elite Tissue Oximetry Cable recall
  FDA September 30, 2026 · Becton Dickinson & Co. · Class II
• Medline convenience kits containing Healthmark Instrument Channel Brushes recall
  FDA September 30, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Healthmark Instrument Channel Brushes recall
  FDA September 30, 2026 · Medline Industries, LP · Class II
• REF:B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• REF:B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• REF:B12LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• REF:B11LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/STABILITY… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• REF:2B5LT Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW… recall
  FDA September 23, 2026 · Stryker Sustainability Solutions · Class II
• HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT… recall
  FDA September 23, 2026 · Wilson-Cook Medical Inc. · Class II
• Happiest Baby, Inc recall
  FDA September 23, 2026 · Happiest Baby, Inc · Class II
• Happiest Baby, Inc SNOO Sleep Sack, X-Small Model recall
  FDA September 23, 2026 · Happiest Baby, Inc · Class II
• IV Sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• IV Sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• IV Sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• IV Sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• Oncology sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• Oncology sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• IV Non-Dedicated Gravity Administration Sets with drip chambers recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• Plum administration sets recall
  FDA September 23, 2026 · ICU Medical, Inc. · Class II
• Philips PIC iX Essentials recall
  FDA September 23, 2026 · Philips North America Llc · Class II
• Philips Patient Information Center iX recall
  FDA September 23, 2026 · Philips North America Llc · Class II
• BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD… recall
  FDA September 23, 2026 · Bd Switzerland Sarl · Class I
• DuoGlide Short-Term Straight Dialysis Catheter recall
  FDA September 23, 2026 · Bard Access Systems, Inc. · Class I
• Power-Trialysis Short-Term Straight Dialysis Catheter recall
  FDA September 23, 2026 · Bard Access Systems, Inc. · Class I
• HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes:… recall
  FDA September 16, 2026 · HeartSine Technologies Ltd · Class II
• Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Products that contain the Pericare Wipes: SureStep" Foley Tray System… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Products that contain the Pericare Wipes: SureStep Intermittent Catheter… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Products that contain the Pericare Wipes: *Bardex¿ I.C… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter… recall
  FDA September 16, 2026 · C.R. Bard Inc · Class II
• Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL recall
  FDA September 9, 2026 · Baxter Healthcare Corporation · Class II
• Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS recall
  FDA September 9, 2026 · Baxter Healthcare Corporation · Class II
• HEALON EndoCoat PRO recall
  FDA September 9, 2026 · Johnson & Johnson Surgical Vision, Inc. · Class II
• Halyard medical convenience kits labeled as: 1) A-P PACK - 205936… recall
  FDA September 9, 2026 · AVID Medical, Inc. · Class II
• 1) NEURO, (kit) ACNE73-01 recall
  FDA September 9, 2026 · AVID Medical, Inc. · Class II
• Halyard medical convenience kits labeled as: 1) ENT… recall
  FDA September 9, 2026 · AVID Medical, Inc. · Class II
• Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl recall
  FDA September 2, 2026 · Byron White Formulas, Inc. · Class II
• Byron White FORMULAS A-P Herbal Supplement 1.0 fl recall
  FDA September 2, 2026 · Byron White Formulas, Inc. · Class II
• Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl recall
  FDA September 2, 2026 · Byron White Formulas, Inc. · Class II
• bettergoods brand Pistachio Nut Butter, NET WT 6.7oz (190g) recall
  FDA September 2, 2026 · Botticelli Foods, LLC · Class I
• Dentsply Sirona Capsule Mixer Model No recall
  FDA August 26, 2026 · SDI Limited · Class II
• 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code:… recall
  FDA August 19, 2026 · Bd Switzerland Sarl · Class II
• ERBECRYO 2 Cryosurgical Unit Model recall
  FDA August 19, 2026 · Erbe USA Inc · Class II
• Xhibit Product Name: Xhibit Central Station Model recall
  FDA August 19, 2026 · Spacelabs Healthcare, Inc. · Class II
• navify Digital Pathology (on-prem) v2.5, Material Number 10092343001… recall
  FDA August 19, 2026 · Ventana Medical Systems, Inc. · Class II
• BOBBY Balloon Guide Catheter recall
  FDA August 19, 2026 · Microvention Inc. · 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