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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
December 31, 2025Food & BeverageFDA
Mellace Family Brands California Inc recalls 1) Wegmans Deluxe Mixed Nuts, Unsalted, Net Wt. 34 oz. (964g), packaged in a plastic tub with UPC 077890421314, packed 6
Hazard: Potential contamination with Salmonella
December 31, 2025Food & BeverageFDA
First & Last Tavern recalls First & Last Tavern Puttanesca Sauce (olives, capers, hot peppers) 26 FL OZ (1 lb, 10 oz) 737g
Hazard: May be contaminated with Clostridium botulinum
December 31, 2025Food & BeverageFDA
First & Last Tavern recalls First & Last Tavern Marinara Sauce (tomato & basil) 26 FL OZ (1 lb, 10 oz) 737g
Hazard: May be contaminated with Clostridium botulinum
December 31, 2025Food & BeverageFDA
First & Last Tavern recalls First & Last Tavern Traditional Pasta Sauce (meat flavored) 26 FL OZ (1 lb., 10 oz) 737g
Hazard: May be contaminated with Clostridium botulinum
December 31, 2025Food & BeverageFDA
Wegmans Food Markets, Inc. recalls Locatelli Pecorino Romano Cheese Grated (Wegmans #270010) Packaged and sold by the pound Packaged in cylindrical clear p
Hazard: Product may be contaminated with Listeria monocytogenes.
December 31, 2025Food & BeverageFDA
Karabetian Import and Distribution, Inc. recalls Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 520
Hazard: partially hydrogenated oils (PHOs) in foods exported to the US
December 31, 2025Food & BeverageFDA
Karabetian Import and Distribution, Inc. recalls Product: Zimi Puff Pastry French Style (frozen) Package Size and quantity per case: 700 g paper carton - 12/case UPC: 5
Hazard: partially hydrogenated oils (PHOs) in foods exported to the US
December 31, 2025Food & BeverageFDA
The James Skinner LLC recalls Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid w
Hazard: Undeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label.
December 31, 2025Food & BeverageFDA
Mondelez Global Llc recalls Ritz Peanut Butter Cracker Sandwiches, Net Wt. 27.6 oz.- 20 Count (20 x 1.38-oz. 6-pack carton)
Hazard: Undeclared allergens (Peanut) due to mispackaging
December 31, 2025Food & BeverageFDA
Bell Industries LLC recalls Zen Cleanse Blend herbal tea; .95 oz (27g) pouch; 18 pouches/box UPC: 819005011504
Hazard: Potential Salmonella contamination
December 31, 2025Food & BeverageFDA
Lil Turtles LLC recalls Grandma Belle's Tomato Basil Soup, Net Wt. 17 oz. (482g), packaged in a glass jar, UPC 810084612293, Made By: Lil' Turtl
Hazard: Undeclared allergen - milk
December 31, 2025DrugsFDA
Merck Sharp & Dohme LLC recalls Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufacture
Hazard: Presence of particulate matter: potential presence of metal particulates in the product.
December 31, 2025DrugsFDA
Merck Sharp & Dohme LLC recalls Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme L
Hazard: Presence of particulate matter: potential presence of metal particulates in the product.
December 31, 2025VehiclesNHTSA
Braun Ambulances 2021–2026 Electrical System recall
Hazard: A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. A loss of patient support systems can delay care, increasing the risk of injury.
December 29, 2025VehiclesNHTSA
Gillig 2025 Suspension recall
Hazard: Damaged axle components can decrease stability or vehicle control, increasing the risk of a crash.
December 24, 2025Medical DevicesFDA
Abbott Laboratories recalls Alinity ci-series System Control Module (SCM), REF: 03R70-01, 03R70-20
Hazard: Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the recall is potential performance issues found in the Alinity ci-series System software versions 3.6.1. and lower that could lead to erroneous results for multiple analytes. The issue was identified by Abbott during the internal testing of complaint investigations.
December 24, 2025Medical DevicesFDA
Cepheid recalls Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-10
Hazard: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.
December 24, 2025Medical DevicesFDA
Cepheid recalls Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10
Hazard: Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.
December 24, 2025Medical DevicesFDA
Medtronic MiniMed, Inc. recalls InPen App, Model/CFN Number: MMT-8061 (Android Users)
Hazard: When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow notifications to override phone settings when on mute/Do Not Disturb, and previously set up override permission is deleted, so audible and vibratory notifications not received, which may lead to delayed insulin therapy, hyperglycemia.
December 24, 2025Medical DevicesFDA
Smith & Nephew, Inc. recalls BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener.
Hazard: Removal of affected lot of screws due to labeling error.
December 24, 2025Medical DevicesFDA
Myofunctional Research Company USA recalls Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouth
Hazard: Due to firm mistakenly distributing product within the U.S. without FDA premarket clearance/approval.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-20-PK Sof
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-16-PK Sof
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Sof
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK Pro
Hazard: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number: 502-103 - Calf Implant style 1 size 3
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Pectoral Implant Product Name: Pectoral Implant Model/Catalog Number: 500-106-5 Pectoral Implant sty
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
December 24, 2025Medical DevicesFDA
DSAART LLC recalls Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Number: 401-202-5 Malar Implant style 2 size
Hazard: Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.