Recalls published in October 2025
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in October 2025, newest first.
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Highest risk · 1+ years ago
Lifepro Fitness Bioremedy Infrared Sauna Blankets recall: Risk of Burn Injuries
Risk of Burn Injuries
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Highest risk · 1+ years ago
Mobility Source Medical Technology Co., Ltd Leachoi Bed Rail recall: The recalled bed rails violate the mandatory standard for adult portable bed
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become…
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Highest risk · 1+ years ago
J & D Brush Bio Ionic Hair Curling Irons recall: Burn Hazard
Burn Hazard
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Highest risk · 1+ years ago
Cranach Hardware Tip Restraint Kits recall: Tip-Over Hazard; Manufactured by Cranach Hardware
Tip-Over Hazard; Manufactured by Cranach Hardware
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Highest risk · 1+ years ago
Bealife 5-Drawer Dressers recall: The recalled dressers are unstable if they are not anchored to a wall
The recalled dressers are unstable if they are not anchored to a wall, posing serious tip-over and entrapment hazards that can result in injuries or…
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Highest risk · 1+ years ago
3M Company Thermal Laminators recall: Overheating
Overheating
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Microvention Inc. Flow Re-Direction Endoluminal Devices: Fred 27 recall: Flow diverter may have a manufacturing issue related to the tantalum length
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be…
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Class I · 1+ years ago
Boston Scientific Corporation Accolade DR SL MRI recall: Software to enhance Safety Architecture is available and designed to prevent
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery…
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Class I · 1+ years ago
Bronchovideoscope Olympus BF-Q170 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Extension SET recall: IV sets may leak
IV sets may leak.
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Class I · 1+ years ago
Abbott TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DF recall: Abbott has become aware of a limited number of tip detachment events during
Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
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Class I · 1+ years ago
Boston Scientific Corporation recall: Software to enhance Safety Architecture is available and designed to prevent
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class I · 1+ years ago
OES Bronchofiberscope Olympus BF Type MP60 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class I · 1+ years ago
Boston Scientific Corporation Proponent DR SL recall: Software to enhance Safety Architecture is available and designed to prevent
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class II · 1+ years ago
BioPro Femoral Head Product ID/Description 19023 Head Femoral Ceramic recall: Potential packaging issue that could compromise the sterile barrier. Defect
Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk…
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Class II · 1+ years ago
Boston Scientific Corporation CX Preconnect with Tenacio Pump with InhibiZone recall: The potential for devices to experience inflation and/or deflation
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
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Class I · 1+ years ago
Evis Exera II Bronchovideoscope Olympus BF Type Q180 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class I · 1+ years ago
Boston Scientific Corporation Accolade SR SL MRI recall: Software to enhance Safety Architecture is available and designed to prevent
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…
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Class I · 1+ years ago
Evis Exera II Bronchovideoscope Olympus BF Type 1TQ180 recall: Additional IFU updates to provide further clarification on safe and effective
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma…
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Class II · 1+ years ago
American Contract Systems Inc. Medical convenience kits recall: Identified products were re-gassed (sterilized more than once) after
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection…