Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

19576–19600 of 39605

SevereFDA (Devices)·Z-3231-2017·2017-10-04
Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk
Sorin Group is recalling 72 Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Product
Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3167-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fixation Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling ECT Internal Fixation Drill Bits because raw material anomalies may cause the instruments to fracture during use.
Product
ECT Internal Fixation Drill Bits 2.5 mm Diameter (0.98 Inch), Item Number/EDI 00231802506, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3158-2017·2017-10-04
Zimmer Biomet Recalls M/DN Intramedullary Fixation Distal Drill Pilot Tips
Zimmer Biomet is recalling 182 M/DN Intramedullary Fixation Distal Drill Pilot Tips due to raw material anomalies that may increase the risk of instrument fracture.
Product
M/DN Intramedullary Fixation Distal Drill Pilot Tip 3.2 mm Diameter, Item Number/EDI 00225503332, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V617000·2017-10-04
Hyundai Sonata Seat Belt Linkage Recall for Detachment Risk
Hyundai is recalling 2011-2015 Sonata and Sonata Hybrid vehicles previously repaired under a prior campaign because seat belt linkages may detach from pretensioners, increasing injury risk in a crash.
Product
HYUNDAI — HYUNDAI SONATA HYBRID, SONATA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3228-2017·2017-10-04
Sorin Platinium VR ICDs Recalled for Potential Overconsumption Risk
Sorin Group is recalling Platinium VR implantable cardioverter defibrillators due to a possibility of overconsumption following electrostatic discharge or MRI scans.
Product
Platinium VR 1210, Model Number TDF031U, UDI/GTIN 08031527015514, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3187-2017·2017-10-04
Zimmer Biomet Recalls ECT Quick-Connect Drills Due to Fracture Risk
Zimmer Biomet is recalling 62 ECT Internal Fracture Fixation Quick-Connect Drills because raw material anomalies may cause the instruments to fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 3.5 mm Diameter 11 cm Length, Item Number/EDI 00241003500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V619000·2017-10-04
Lexus Recalls 2010 HS 250h Hybrid for Transaxle Short Circuit Risk
Toyota is recalling 2010 Lexus HS 250h Hybrid vehicles because a hybrid transaxle component may short circuit, causing a loss of power and increasing crash risk.
Product
LEXUS — LEXUS HS 250 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-3606-2017·2017-10-04
Country Fresh Tri-Pepper Dice Recalled for Listeria Contamination Risk
Country Fresh Products is recalling Tri-Pepper Dice due to potential Listeria monocytogenes contamination. Consumers in five states should discard the product.
Product
Tri-Pepper Dice, 6-oz. packaged in a clamshell and Dice Tri-Pepper, 7-oz. packaged in a clamshell
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-3191-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Product
Drill Bit Jacobs Chuck 3.2 mm Diameter 130 mm Length, Item Number/EDI 00480513032, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3188-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drill Bits
Zimmer Biomet is recalling 10 units of ECT Internal Fracture Fixation Quick-Connect Drills due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
ECT Internal Fracture Fixation Quick-Connect Drill 4.0 mm Diameter 20cm Length, Item Number/EDI 00241004000, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3157-2017·2017-10-04
Zimmer Biomet Recalls NCB Periprosthetic Plate System Drill Bits
Zimmer Biomet is recalling 185 NCB Periprosthetic Plate System Drill Bits due to a raw material anomaly that may increase the risk of instrument fracture during use.
Product
NCB Periprosthetic Plate System Drill Bit With Quick-Coupling 4.5 mm Diameter 195 mm Length, Item Number/EDI 0200024330, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·17V620000·2017-10-04
Grand Design Recalls 2017-2018 Imagine Trailers for Fire Risk
Grand Design RV is recalling 2017-2018 Imagine recreational trailers because air conditioning wires may detach and short circuit, increasing fire risk.
Product
GRAND DESIGN — GRAND DESIGN IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3150-2017·2017-10-04
Zimmer Biomet Recalls ECT Internal Fracture Fixation Quick-Connect Drills
Zimmer Biomet is recalling 4 units of ECT Internal Fracture Fixation Quick-Connect Drills due to raw material anomalies that may increase the risk of instrument fracture.
Product
ECT Internal Fracture Fixation Quick-Connect Drill, 1.5 mm Diameter, 85mm Length, Item Number/EDI 00241001500, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-3581-2017·2017-10-04
Country Fresh Vegetable Kabob Recall for Listeria Contamination
Country Fresh Products is recalling specific vegetable kabob products due to potential contamination with Listeria monocytogenes.
Product
Vegetable Kabob, 23-oz. packaged in an overwrap; Kabob Sensations Veggie Kabob, 15-oz. packaged in am overwrap; Marketside Veggie Kabobs, 23-oz. packaged in an overwrap
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-3178-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Screw Taps Due to Material Anomaly
Zimmer Biomet is recalling 198 nonsterile orthopedic screw taps because raw material anomalies may increase the risk of instrument fracture during use.
Product
Zimmer Periarticular Locking Plate System, Locking Screw Tap Standard Quick-Connect 3.5 mm Diameter, Item Number/EDI 00236015335, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3160-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Instruments Due to Fracture Risk
Zimmer Biomet is recalling 21 units of M/DN Intramedullary Fixation Femoral Drills because raw material anomalies may cause the instruments to fracture during use.
Product
M/DN Intramedullary Fixation Femoral Drill Large 5.0 mm Item Number/EDI 00225503550, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3180-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Surgical Drills Due to Fracture Risk
Zimmer Biomet is recalling 1,091 nonsterile orthopedic surgical drills and screw taps because raw material anomalies may cause instrument fracture.
Product
Zimmer Periarticular Locking Plate System Drill Standard 2.0 mm Diameter, Item Number/EDI 00236017520, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-3193-2017·2017-10-04
Zimmer Biomet Recalls Orthopedic Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because a raw material anomaly may increase the risk of instrument fracture during use.
Product
Drill Bit Quick-Connect 2.0 mm Diameter 100 mm Length, Item Number/EDI 00480610020, Nonsterile. orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
SevereUSDA FSIS·106-2017·2017-10-04
Thompson's Ground Beef Recalled for Possible E. coli O157:H7 Contamination
Clair D. Thompson & Sons, Inc. is recalling approximately 700 pounds of ground beef products due to possible E. coli O157:H7 contamination.
Product
Clair D. Thompson & Sons, Inc. Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
2 states
SevereNHTSA·17V616000·2017-10-03
Braun Recalls 2016 BraunAbility MXV Vehicles Due to Airbag Sensor Defect
Braun is recalling 2016 BraunAbility MXV wheelchair accessible vehicles because a seat position sensor may dislodge, potentially causing the frontal airbag to deploy with improper force.
Product
BRAUN — BRAUN BRAUNABILITY MXV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V615000·2017-10-03
Great Dane Recalls 2018 Everest Trailers Due to Brake Caliper Bolt Issue
Great Dane is recalling 2018 Everest trailers because brake caliper bolts may not be properly torqued, which could cause the caliper to detach and result in a loss of braking ability.
Product
GREAT DANE — GREAT DANE EVEREST SS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V614000·2017-10-02
Trail King Recalls 2018 Fifth-Wheel Trailers Due to Brake Caliper Bolt Issue
Trail King is recalling 2018 Fifth Wheel Live Bottom trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.
Product
TRAIL KING — TRAIL KING FIFTH-WHEEL LIVE BOTTOM
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17E055000·2017-10-02
IMMI Recalls School Bus Seats Due to Fracturing Buckle Mount Rods
Indiana Mills and Manufacturing is recalling Generation IV school bus seats because the buckle mount rods may fracture, increasing injury risk in crashes.
Product
SEAT BELTS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V611000·2017-10-02
Forest River Recalls 2013-2014 Coachmen Freedom Express Trailers for Frame Defect
Forest River is recalling 2013-2014 Coachmen Freedom Express trailers because missing frame reinforcements may cause axle misalignment, increasing crash risk.
Product
COACHMEN — COACHMEN FREEDOM EXPRESS
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·103-2017·2017-09-29
Belmont Sausage Recalls Smoked Turkey Drumsticks Due to Undeclared Milk Allergen
Belmont Sausage Co. is recalling smoked turkey drumsticks because they contain undeclared milk, a known allergen. The products were distributed nationwide via an institutional location in Michigan.
Product
Belmont Sausage Co. Recalls Smoked Turkey Drumstick Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
1 state

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19576–19600 of 39605