Recalls in Vermont (page 18)
3845 recalls.
- Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - PARACENTESIS KIT recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Med Pride recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Cura Hongos recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Rapidol recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lil Drug Store recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Circle K recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Lucky Super Soft recall (Dabur India Limited)
DrugClass IIReported June 24, 2026 · CGMP Deviations; deficiencies observed during FDA inspection - Chlorthalidone Tablets recall (Inventia Healthcare Limited)
DrugClass IIReported June 24, 2026 · Failed Dissolution Specifications - Focalin XR recall (Sandoz Inc)
DrugClass IIIReported June 24, 2026 · Labeling: Incorrect or Missing Lot and/or Exp Date - safco SensiCaine-Ultra recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - PureLife recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Dental City TOPICAL ANESTHETIC GEL recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Burkhart topical anesthetic gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - DHP Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Quala Dental Products recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Pearson Quality Topical Anesthetic Gel recall (Keystone Industries)
DrugClass IIReported June 24, 2026 · Defective container:may contain bottles with incomplete seals - Buprenorphine HCl recall (Par Health USA, LLC)
DrugClass IIReported June 24, 2026 · Crystallization; identified as Buprenorphine free base - Aripiprazole Tablets USP recall (Ajanta Pharma USA Inc)
DrugClass IIReported June 24, 2026 · Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg. - Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride recall (IntegraDose Compounding Services LLC)
DrugClass IIReported June 24, 2026 · Subpotent Drug - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - VistaPharm recall (PAI Holdings LLC)
DrugClass IIReported June 24, 2026 · Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023 - Alyacen 7/7/7 recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported June 24, 2026 · Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities. - Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog... recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System recall (Thoratec LLC)
Medical deviceClass IIReported June 24, 2026 · Due to 11 volt Backup Battery failures. - Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 ... recall (Merit Medical Systems, Inc.)
Medical deviceClass IIReported June 24, 2026 · Due to unsealed portions of pouches. - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product... recall (Staar Surgical AG)
Medical deviceClass IIReported June 24, 2026 · Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses. - MEDLINE Medical Procedure Kits labeled as: 1) CRANI recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) RETINA LAC/USC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) D AND C PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BASIC GYN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CAROTID NEURO PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: NURSING KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: DR FERNANDEZ recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CV DRAPING/BASIN recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: TONSIL PACK CATH recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) CHEST EXPLORATION ECMO recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: BILAT MICRO VASECTOMY REVERSAL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as CH OPEN HEART recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Medical Procedure Kits labeled as: LAPAROSCOPY COMBINED - NO NDL recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Pre-connected Urethral Catheterization Tray and Bag recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheterization Tray recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - MEDLINE Urethral Catheter recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include... - Giraffe OmniBed Field Replaceable Unit recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1 recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - Giraffe OmniBed recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 24, 2026 · GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for... - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip recall (ConMed Corporation)
Medical deviceClass IIReported June 24, 2026 · Potential for overpressure alerts. - TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300. recall (Howmedica Osteonics Corp.)
Medical deviceClass IIReported June 24, 2026 · Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot... - Medtronic O-arm O2 Imaging System. Model Number: BI70002000. recall (Medtronic Navigation, Inc.-Boxborough)
Medical deviceClass IIReported June 24, 2026 · Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware. - ALYON Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. - HarmonyAIR A-Series Surgical Lighting System recall (Steris Corporation)
Medical deviceClass IIReported June 24, 2026 · There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. - Medline convenience kits: HYSTERECTOMY PACK-LF DYNJ20485L recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D ... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for... - Medline convenience kits: ADD-A-CATH ARTERIAL INSERTION ARTNC185 PED SCHOOL AGE... recall (Medline Industries, LP)
Medical deviceClass IIReported June 24, 2026 · Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for...