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 deaths or serious injuries are reported, 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

3276–3300 of 5111

SevereFDA (Devices)·Z-2419-2018·2018-07-18
Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy
Medtronic is recalling 8,821 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.
Product
Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular def
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2400-2018·2018-07-18
Stryker Recalls Femoral Nails Due to Potential Premature Breakage
Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.
Product
Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
Category
Medical Device
Distribution
8 states
SevereFDA (Devices)·Z-2347-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter may damage implanted leads if over-tightened, potentially requiring replacement.
Product
microTargeting" Drive System, Product Number 66-ZD-MD
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2346-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Lead and Stylet Damage
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage implanted leads and stylets when over-tightened, requiring device replacement.
Product
microTargeting" Drive System, Product Number MT-DS-01
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2352-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, causing short circuits and requiring replacement.
Product
microTargeting" STar" Drive System (Motorized), Product Number 70-ZD-ME
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2350-2018·2018-07-11
FHC Depth Stop Adapter Recall Due to Lead and Stylet Damage
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads and stylets, requiring replacement.
Product
microTargeting" STar" Drive System (Motorized), Product Number ST-DS-ME
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2351-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage the implanted lead, requiring removal and replacement.
Product
microTargeting" STar" Drive System (Manual), Product Number 70-ZD-MA
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2355-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System Distributed by Medtronic, Product Number FC1006
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2359-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Lead Damage Risk
FHC, Inc. is recalling Depth Stop Adapters because over-tightening the screw can damage implanted leads, requiring removal and replacement.
Product
microtargeting" Depth Stop Adapter, Product Model Number, Product Number 66-AC-DS(1.8),
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2358-2018·2018-07-11
FHC Depth Stop Adapter Recall Due to Lead Damage Risk
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring surgical replacement.
Product
microTargeting" STar" Drive System (Motorized) Distributed by Medtronic, Product Number FC8002
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2349-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead Damage
FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter may damage the lead and stylet if the screw is over-tightened.
Product
microTargeting" STar" Drive System (Manual), Product Number ST-DS-MA
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2356-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Potential Lead and Stylet Damage
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System Distributed by Medtronic, Product Number 9033G0601
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2293-2018·2018-07-11
Howmedica Recalls LFIT Anatomic CoCr Femoral Heads Due to Disassociation
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
Product
LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-040
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2345-2018·2018-07-11
FHC microTargeting Drive System Recalled for Lead Damage Risk
FHC, Inc. is recalling 2,952 microTargeting Drive Systems because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Product
microTargeting" Drive System, Product Number MT-DS
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2354-2018·2018-07-11
FHC Depth Stop Adapter Recall for Potential Lead Damage
FHC, Inc. is recalling microTargeting Lead Adapters because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Product
microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2348-2018·2018-07-11
FHC Depth Stop Adapter Recalled for Lead and Stylet Damage
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage leads and stylets, potentially causing short circuits.
Product
microTargeting" Drive System, Product Number 66-ZD-MD-01
Category
Medical Device
Distribution
46 states
SevereFDA (Devices)·Z-2302-2018·2018-07-04
Intersurgical Flexible Breathing Circuit Recall Due to Exhalation Port Blockage Risk
Intersurgical Inc is recalling 1,340 Flexible Smoothbore Breathing Circuits because the tubing may block the exhalation port during assembly, posing a serious health risk to patients.
Product
Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Category
Medical Device
Distribution
5 states
SevereFDA (Devices)·Z-2300-2018·2018-07-04
Philips OmniDiagnost-Eleva X-ray System Recalled Due to Table Rotation Hazard
Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.
Product
OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2301-2018·2018-07-04
Philips OmniDiagnost X-ray System Recalled for Tilt Actuator Failure Risk
Philips is recalling 477 OmniDiagnost Classic X-ray systems because a broken tilt actuator could cause the table to rotate uncontrollably, posing a risk of injury.
Product
OmniDiagnost Classic X-ray system Angiographic and Diagnostic, Product Nos. 70859, 708023, 708024, 708025
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2281-2018·2018-07-04
Konica Minolta CS-7 Medical Device Recall Due to Laptop Fire Risk
Konica Minolta is recalling CS-7 medical devices because the Panasonic Toughbook laptops used in some configurations have a potential battery ignition risk.
Product
CS-7, Model No. A4C1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2282-2018·2018-07-04
Konica Minolta ImagePilot D9MA Recalled for Potential Laptop Battery Fire Risk
Konica Minolta is recalling ImagePilot D9MA units because the Panasonic Toughbook laptops used in some configurations may experience battery ignition.
Product
ImagePilot, Model No. D9MA
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2251-2018·2018-06-27
Draeger Fabius GS Tiro Anesthesia Machine Recalled for Hypoxia Risk
Draeger Medical is recalling 31 Fabius GS Tiro anesthesia machines because a fault could allow 100% nitrous oxide delivery, creating a risk of hypoxic mixtures and patient death.
Product
Fabius GS Tiro Anesthesia Machine; Cat. no. 8606000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fabiu
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2252-2018·2018-06-27
Draeger Fabius GS MRI Anesthesia Machine Recalled for Hypoxia Risk
Draeger Medical is recalling four Fabius GS MRI Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients, potentially causing death.
Product
Fabius GS MRI Anesthesia Machine; Cat. no. 8607300 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fabius
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2250-2018·2018-06-27
Draeger Fabius GS Premium Anesthesia Machine Recalled for Hypoxia Risk
Draeger Medical is recalling 62 Fabius GS Premium Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients.
Product
Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders. Fa
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2253-2018·2018-06-27
Draeger Apollo Anesthesia Machine Recalled for Potential Hypoxic Gas Delivery
Draeger Medical is recalling 72 Apollo Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients, posing a risk of death.
Product
Apollo Anesthesia Machine; Cat. no. 8605310 Product Usage: Indicated as a continuous flow anesthesia system. The Apollo may be used for manually assisted or automatic ventilation, delivery of gases and anesthetic vapor, and monitoring of oxygen and CO2 concentration, breathin
Category
Medical Device
Distribution
Distributed nationwide

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3276–3300 of 5111