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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,ATRIAL RETRACTOR SHORT RIGHT,IS4000¿ REF 470246
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,LARGE HEM-O-LOK CLIP APPLIER,IS4000¿ REF 470230
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,TENACULUM FORCEPS,IS4000¿ REF 470207
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,FENESTRATED BIPOLAR FORCEPS,IS4000¿ REF 470205
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,MEGA NEEDLE DRIVER,IS4000¿ REF 470194
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,RESANO FORCEPS,IS4000 ¿ REF 470181
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,MARYLAND BIPOLAR FORCEPS,IS4000 ¿ REF 470172
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,MICRO BIPOLAR FORCEPS,IS4000 ¿ REF 470171
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,PROGRASP FORCEPS,IS4000 ¿ REF 470093
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,CADIERE FORCEPS,IS4000 ¿ REF 470049
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,DEBAKEY FORCEPS,IS4000 ¿ REF 470036
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM,BLACK DIAMOND MICRO FORCEPS,IS4000 ¿ REF 470033
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM, ROUND TIP SCISSORS, IS4000 ¿ REF 470007
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM, LARGE NEEDLE DRIVER, IS4000 REF 470006
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM, POTTS SCISSORS, IS4000 REF 470001
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Intuitive Surgical, Inc. recalls 8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Hazard: Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
January 22, 2025Medical DevicesFDA
Tornier S.A.S. recalls Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder Arthro
Hazard: The Pin Guide is being recalled because the metal tube may disassemble from the plastic handle. This can result in the Blueprint Mixed Reality headset being unable to detect the Pin Guide and potentially prolonging surgery time or changing of surgical method from guided to conventional.
January 22, 2025Medical DevicesFDA
Coloplast Manufacturing US, LLC recalls X-Flow prostatectomy catheter, Device Reference Numbers AB6022, AB6024, AB6118, AB6120, AB6122, AB6124, AB6220, AB6222,
Hazard: A possible sterility issue was detected in Coloplast's facility on some Coloplast products.
January 22, 2025Medical DevicesFDA
Coloplast Manufacturing US, LLC recalls Folysil Silicone Foley Catheters, Device Reference Numbers AA6106, AA6108, AA6110, AA6112, AA6114, AA6116, AA6118, AA612
Hazard: A possible sterility issue was detected in Coloplast's facility on some Coloplast products.
January 22, 2025Medical DevicesFDA
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC77V;
Hazard: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
January 22, 2025Medical DevicesFDA
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC71V;
Hazard: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
January 22, 2025Medical DevicesFDA
Augustine Temperature Management, LLC recalls Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses
Hazard: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
January 22, 2025Medical DevicesFDA
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # W
Hazard: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
January 22, 2025Medical DevicesFDA
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) Model # W
Hazard: HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
January 22, 2025Medical DevicesFDA
NOA Medical Industries Inc recalls NOA Medical Industries Behavioral Health Hospital bed side rails, Product number 1055050GRY-BOX
Hazard: Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.
January 22, 2025Medical DevicesFDA
Karl Storz Endoscopy recalls Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Hazard: Due to failure of manual cleaning validation, biopsy and grasping forceps like sterility assurance.
January 22, 2025Medical DevicesFDA
Biocartis Nv recalls Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human samples
Hazard: False-positive MSI-H results generated by the Idylla MSI Test.
January 22, 2025Medical DevicesFDA
Alcon Research LLC recalls Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Descripti
Hazard: Increase in complaints associated with a molding defect within the inner lumen of delivery cartridges which could result in a scratch on the intraocular lens (IOL) upon delivery.
January 22, 2025Medical DevicesFDA
Cook Biotech, Inc. recalls Cook Medical Biodesign Dural Graft, REF C-DUR-7X10, REF G31091, Sterile
Hazard: Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.
January 22, 2025Medical DevicesFDA
Cook Biotech, Inc. recalls Cook Medical Biodesign Hiatal Hernia Graft, REF C-PHR-7X10-U, REF G31455, Sterile; and
Hazard: Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.