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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical 73" (185 cm) Appx 2.5 ml, Ext Set, Smallbore w/ChemoLock Port, Clamp, ChemoLock w/Red Cap REF: CL4176
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical 60" (152 cm) Appx 1.2 ml, Ext Set, Smallbore w/ChemoLock Port, Clamp, Spiros w/Red Cap REF: CL4173
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical 45" (114 cm) Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap, Anti-Siphon Valve, Clamp, Y-Connector w/Che
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Oncology Transfer Kit w/ChemoClave and ChemoLock Port; Spiros w/Red Cap; ChemoLock Port REF: CL4138
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Oncology Kit w/ChemoLock, ChemoLock Port REF: CL4136
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical ChemoLock Bag Spike with Clave Additive Port REF: CL3940
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Oncology Kit w/31" (79 cm) 20 Drop Admin Set w/Integrated ChemoLock" Port Drip Chamber, Spiros"; ChemoLock"
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical 30" (76 cm) Appx 3.6 ml, 20 Drop Admin Set w/Integrated ChemoLock Port Drip Chamber, ChemoLock w/Red Cap,
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical 30" (76 cm) Appx 3.3 mL, Admin Set w/20 Drop Integrated ChemoLock Drip Chamber, Spiros", Hanger, Drop-In Re
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Clave Bag Spike w/ChemoLock Port REF: CL2150
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical ChemoLock" Port, Bulk, Non-Sterile REF: CL2100-NS
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ICU Medical Chemo Lock Universal Vented Vial Spike REF: CL-70-10
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
ICU Medical, Inc. recalls ChemoLock Bag Spike, 01 units REF: CL-10-10
Hazard: Port weld of drug transfer device may separate or break during use and potentially result in a leak.
November 5, 2025Medical DevicesFDA
Canon Medical System, USA, INC. recalls VANTAGE GALAN 3T. CMSC Model: MRT-3020/U7. Model Number: MEXL-3020/B7.
Hazard: Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrical equipment.
November 5, 2025Medical DevicesFDA
Alcon Research LLC recalls Alcon PRECISION1 One-Day Contact Lenses, -2.25D.
Hazard: Potential for a weak seal in some units resulting in compromise in sterility.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls Surgical Planner, BrainSTORM, software version BST.9.3.0, orthopedic augmented reality
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls SpineAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SPR.1.2.0, orthopedic a
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls Endo Surgical Navigation Advanced Platform Patient Engagement (EndoSNAP), software version SNP.1.12.0, imaging processin
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls SyncAR Surgical Navigation Advanced Platform Patient Engagement (SyncAR SNAP), software version SNP.1.12.0, imaging proc
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls Surgical Navigation Advanced Platform Patient Engagement (PE SNAP), software version SNP.3.12.0, imaging processing radi
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls Surgical Navigation Advanced Platform (SNAP), software version SNP.3.12.0, imaging processing radiological system
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Surgical Theater Inc recalls SuRgical Planner (SRP), software version SRP.7.12.0, imaging processing radiological system
Hazard: A software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any secondary image layer(s) to the primary image layer.
November 5, 2025Medical DevicesFDA
Dexcom, Inc. recalls Brand Name: Dexcom G6 Continuous Glucose Monitoring System Product Name: Dexcom G6 and G6 Pro Android US CGM App Model
Hazard: A software defect in version v1.15.0 of the G6 Android app can cause the app to terminate unexpectedly, which may result in the user not receiving estimated glucose values, alarms, alerts or notifications. This could result in the missed detection of a hyperglycemic or hypoglycemic event, protentional resulting in severe hyperglycemia, diabetic ketoacidosis (DKA), or hyperosmolar hyperglycemic state (HHS).
November 5, 2025Medical DevicesFDA
ENDOMAGNETICS LTD recalls Magseed Pro 12 cm soft tissue marker. Model Number: MS2-17-1-12. Product Description: The Endomag Magseed Pro Magneti
Hazard: Potential for contamination with cotton fibers.
November 5, 2025Medical DevicesFDA
ENDOMAGNETICS LTD recalls Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic
Hazard: Potential for contamination with cotton fibers.
November 5, 2025Medical DevicesFDA
Aesculap Inc recalls Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N
Hazard: It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
November 5, 2025Medical DevicesFDA
Aesculap Inc recalls Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/
Hazard: It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
November 5, 2025Medical DevicesFDA
Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Model/Catalog Number: EK085P Software Version: N/A
Hazard: It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
November 5, 2025Medical DevicesFDA
Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Ver
Hazard: It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
November 5, 2025Medical DevicesFDA
Alcon Research LLC recalls Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Mod
Hazard: Due to incomplete seals in the pouch which provide the sterile barrier.