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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 5, 2025Medical DevicesFDA
Zimmer, Inc. recalls NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
Hazard: It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.
February 5, 2025Medical DevicesFDA
Zimmer, Inc. recalls NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14
Hazard: It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553570
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553550
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553540
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553530
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553520
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 8mmx8mm UPN: M00553690
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN: M00553680
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553670
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553660
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Boston Scientific Corporation recalls AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN: M00553640
Hazard: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
February 5, 2025Medical DevicesFDA
Accuray Incorporated recalls CyberKnife Treatment Delivery System, REF 0660000 The CyberKnife System may be labeled as CyberKnife M6TM or VSI TM R
Hazard: Snap rings may become partially or completed detached from the shafts within the internal mechanism. Uncontrolled rotation may occur on the left and right roll axes when the rings are removed or damaged.
February 5, 2025Medical DevicesFDA
Medtronic Navigation, Inc. recalls Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 Th
Hazard: Due to an increase in complaint that the percutaneous reference pin would not fit into the patient reference frame or percutaneous pin adapter.
February 5, 2025Medical DevicesFDA
B. Braun Medical, Inc. recalls Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal
Hazard: Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore is unable to be used to administer medication.
February 5, 2025Medical DevicesFDA
Instrumentation Laboratory recalls HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic
Hazard: Control indicating lower than expected quality control (QC) results and in some instances QC recovery below the lower limit of the package insert acceptance range.
February 5, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
Hazard: The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
February 5, 2025Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT, Item Number ART1185B; 2) ARTERIAL LINE BUNDLE, I
Hazard: The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
February 5, 2025Medical DevicesFDA
SIEMENS MEDICAL SOLUTIONS USA, INC recalls ARTIS One Angiographic X-Ray System
Hazard: A potential issue with ARTIS One systems was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose-rate may be higher than intended by the user.
February 5, 2025Food & BeverageFDA
Clements Foods Co recalls Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, UPC 046045062467; Red Boy brand mustard,
Hazard: Ingredient (mustard seeds) tested positive for Salmonella
February 5, 2025Food & BeverageFDA
BakeMark USA LLC. recalls WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch, Contain
Hazard: Scheduled process deviation: Final pH of 4.61, 4.66, 4.69, 4.67.
February 5, 2025Food & BeverageFDA
Iovate Health Sciences USA Inc. recalls Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in a
Hazard: Presence of cathine in product
February 5, 2025Food & BeverageFDA
GBC Food Services, LLC dba Yummi Sushi recalls Vegetarian Roll UPC: 85375900869 Qty: 1 Tray, Net Wt: 6.1oz (174g) 11/22 to 11/29/2024 Vegetarian Roll (Brown Rice) UPC:
Hazard: Possible contamination with Salmonella
February 5, 2025Food & BeverageFDA
GBC Food Services, LLC dba Yummi Sushi recalls Karaage Chicken Bao Buns UPC: 85006499045 Net Wt: 8.8 oz (251g) 11/22 to 11/29/2024 Gyoza Combo UPC: 85001442018 Qty: 11
Hazard: Possible contamination with Salmonella
February 5, 2025Food & BeverageFDA
GBC Food Services, LLC dba Yummi Sushi recalls Spicy Salmon Roll UPC: 85375900865 Qty: 1 Tray, Net Wt: 8.1oz (230g) 11/22 to 11/29/2024 Fusion Spring Roll (Salmon) UPC
Hazard: Possible contamination with Salmonella
February 5, 2025Food & BeverageFDA
GBC Food Services, LLC dba Yummi Sushi recalls Tempura Shrimp Roll UPC: 85375900884 Qty: 1 Tray, Net Wt: 10oz (284g) 11/22 to 11/29/2024 Spicy Cajun Shrimp Roll UPC:
Hazard: Possible contamination with Salmonella