Recalls distributed in Rhode Island

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

687 recalls published between October 9, 2024 and September 30, 2026 (686 FDA, 1 CPSC). Most common issues: sterility (103), injury risk (66), microbial contamination (47), undeclared allergen (28). 112 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
• Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30… recall
  FDA September 30, 2026 · WFM Purchasing, LP · Class I
• 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
• 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
• HEALON EndoCoat PRO recall
  FDA September 9, 2026 · Johnson & Johnson Surgical Vision, 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
• Esteem Body Soft Convex Urostomy Pouch Model recall
  FDA August 26, 2026 · ConvaTec, Inc · Class II
• Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2… recall
  FDA August 26, 2026 · Kico Knee Innovation Company · Class II
• Dentsply Sirona Capsule Mixer Model No recall
  FDA August 26, 2026 · SDI Limited · Class II
• EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050… recall
  FDA August 26, 2026 · Covidien, LP · Class II
• Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz recall
  FDA August 26, 2026 · Prospector Popcorn, LLC · Class III
• Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz recall
  FDA August 26, 2026 · Prospector Popcorn, LLC · Class III
• Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz recall
  FDA August 26, 2026 · Prospector Popcorn, LLC · Class III
• Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz recall
  FDA August 26, 2026 · Prospector Popcorn, LLC · Class II
• ERBECRYO 2 Cryosurgical Unit Model recall
  FDA August 19, 2026 · Erbe USA Inc · Class II
• OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source… recall
  FDA August 19, 2026 · OBP Medical Corporation · Class II
• Xhibit Product Name: Xhibit Central Station Model recall
  FDA August 19, 2026 · Spacelabs Healthcare, Inc. · Class II
• GORE VIABIL Short Wire Biliary Endoprosthesis, Model No recall
  FDA August 19, 2026 · W L Gore & Associates, Inc. · Class II
• GORE VIABIL Short Wire Biliary Endoprosthesis, Model No recall
  FDA August 19, 2026 · W L Gore & Associates, Inc. · 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
• 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