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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
Hazard: There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls MEDLINE ANTERIOR HIP PACK DYNJ64672B
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ9
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY K
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls THORACIC ROBOTS, DYNJ908777B
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH P
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Airway Exam Kit, DYKE1796
Hazard: Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
April 8, 2026Medical DevicesFDA
SUMMA THERAPEUTICS, LLC recalls Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251
Hazard: Potential for the balloon in the device to not meet burst specifications.
April 8, 2026Medical DevicesFDA
Synthes (USA) Products LLC recalls 2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
Hazard: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
April 8, 2026Medical DevicesFDA
Synthes (USA) Products LLC recalls 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.
Hazard: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instru
Hazard: Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Mode
Hazard: Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Mo
Hazard: Due to increased complaints for broken/frayed grip cables for reusable instruments.
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Mo
Hazard: Due to increased complaints for broken/frayed grip cables for reusable instruments.
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Graspe
Hazard: Due to increased complaints for broken/frayed grip cables for reusable instruments.
April 8, 2026Medical DevicesFDA
Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scisso
Hazard: Due to increased complaints for broken/frayed grip cables for reusable instruments.
April 8, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog
Hazard: Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
April 8, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/
Hazard: Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable. Additionally, smoke or a burning smell may occur. By design, the issue causing the smoke or burning smell would be contained within the internal laser console enclosure and would be self-extinguishing.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Hazard: There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
April 8, 2026Medical DevicesFDA
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Vue Motion V12. Product Number: 1017979.
Hazard: Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCH
Hazard: Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.
April 8, 2026Medical DevicesFDA
Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Hazard: Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Leakage may result in delayed care and fluid loss. Additional consequences may also occur if user over-tightens the connector to stop the leakage, including additional clinical intervention, risk of infection, patient discomfort, and prolonged recovery process.
April 8, 2026Medical DevicesFDA
Ultradent Products, Inc. recalls Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.
Hazard: Composite polisher cups may crumble and break apart easily, which could cause a delay in patient treatment.
April 8, 2026Medical DevicesFDA
Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Hazard: Surgical light assembly may not adequate support the weight of the ceiling cover.