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

20051–20075 of 27461

HighFDA (Devices)·Z-0752-2023·2022-12-28
GE Vivid S5 Ultrasound Systems Battery Failure Fire Risk
GE Medical Systems is recalling Vivid S5 ultrasound systems because batteries may fail if not replaced at the recommended 2-year intervals, potentially causing smoke or fire.
Product
Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superf
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0735-2023·2022-12-28
Natus Cranial Access Kit Recalled Due to Defective Sterile Surgical Drapes
Natus Medical is recalling 249 Cranial Access Kits distributed nationwide. The sterile surgical drape liners are difficult to remove without damage, potentially rendering the kits unusable for neurosurgical procedures.
Product
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set that is used to create an intracranial burr-hole typically required for procedures such as ventriculostomy or intracranial pressure (ICP) monitoring. The various
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0747-2023·2022-12-28
HeartWare HVAD Pump Kit driveline cover hardening may prevent repairs
A hardened driveline cover on the HeartWare HVAD Pump Kit may prevent or delay access to the driveline to controller connector. If urgent servicing is needed, the delay could result in patient harm from pump malfunction.
Product
HeartWare HVAD Pump Kit, REF 1104CA-CLIN
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0762-2023·2022-12-28
Baxter Revaclear 300 Dialyzers Recalled for Polyurethane Displacement
Baxter is recalling approximately 14 million units of Revaclear 300 dialyzers worldwide due to polyurethane displacement that could cause blood leaks. No injuries have been reported.
Product
Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0753-2023·2022-12-28
GE Vivid S6 Ultrasound Systems Recalled for Battery Fire Risk
GE Vivid S6 ultrasound systems are recalled for a potential battery hazard. If not replaced at the recommended 2-year interval, batteries may fail, emit smoke, or catch fire.
Product
Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superf
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0088-2023·2022-12-28
Prescription Drug Quinapril Recalled for Chemical Impurity Exceeding Safety Limits
Lupin Pharmaceuticals is recalling Quinapril 40mg tablets due to detection of N-Nitroso-quinapril impurity above acceptable daily intake limits. The recall affects approximately 30,612 bottles distributed nationwide.
Product
QUINAPRIL — QUINAPRIL (QUINAPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0766-2023·2022-12-28
Lamaze Chill Teether Recalled for Potential Microbial Growth in Fluid
Lamaze Chill Teether teething rings are being recalled due to potential microbial growth in the internal fluid. This poses an infection risk, particularly for children with weakened immune systems.
Product
Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0751-2023·2022-12-28
FDA Class II recall: Medical Action cardiac catheter introduction kit
Medical Action Industries' Port a Cath Kit (cardiac catheter introduction kit) has been subject to an FDA Class II recall affecting 198 cases distributed in Virginia. The specific reason for recall was not provided by the FDA.
Product
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0746-2023·2022-12-28
HeartWare HVAD Pump Kit Driveline Cover Hardening Issue
HeartWare HVAD Pump Kit driveline covers may harden over time, making it difficult or impossible to access the driveline connector for urgent servicing. Delayed access could result in patient harm from prolonged pump stoppage.
Product
HeartWare HVAD Pump Kit, REF 1104
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0201-2023·2022-12-28
Frozen pizza dough recalled for possible foreign object contamination
It'll Be Pizza frozen pizza dough (20 oz and 24 oz packages) may contain foreign debris from packaging. Consumers should not consume affected products.
Product
20 oz Garlic and 24 oz Garlic frozen pizza dough manufactured by It'll Be Pizza
Category
Food
Distribution
5 states
HighFDA (Drugs)·D-0087-2023·2022-12-28
Glycopyrrolate Tablets Recalled for Failed Impurities and Degradation Specifications
Glycopyrrolate tablets distributed nationwide are being recalled due to failed impurities and degradation specifications. Patients with affected lots should discontinue use and consult their healthcare provider.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0196-2023·2022-12-28
Brava Frozen Pizza Dough Recalled for Possible Foreign Object Contamination
Brava frozen pizza dough products are being recalled due to possible contamination with debris from packaging. The recall affects 1,678 cases distributed in Maine, Vermont, Massachusetts, Pennsylvania, and New Hampshire.
Product
Brava, 20 oz, 22 ct/case and Brava, 24 oz, 18 ct/case frozen pizza dough
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0750-2023·2022-12-28
HeartWare HVAD Pump Kit driveline cover hardening affects connector access
Driveline cover hardening in HeartWare HVAD Pump Kits may prevent access to critical connectors, potentially delaying emergency repairs. Affected patients should contact their Medtronic field representative for assessment.
Product
HeartWare HVAD Pump Kit, REF MCS1705PU
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0738-2023·2022-12-28
Spinal implant insert may fail to disengage from vertebral body device
NuVasive's X-CORE 2 spinal implants may not disengage properly from the vertebral replacement device, potentially requiring revision surgery. About 2,031 devices worldwide are affected.
Product
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0757-2023·2022-12-28
GE Vivid q Ultrasound Systems: Battery Fire Risk Recall
GE is recalling Vivid q ultrasound systems because batteries not replaced every 2 years as recommended may fail and emit smoke or catch fire.
Product
Vivid q ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superfi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0765-2023·2022-12-28
Medical Action Industries Littauer Scissors Recalled for Debris Contamination
Medical Action Industries is recalling Littauer surgical scissors because the sterile instruments may contain debris that could compromise their safety during clinical use.
Product
Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0756-2023·2022-12-28
GE Vivid i Ultrasound Systems Battery Failure Recall
GE Medical Systems is recalling Vivid i ultrasound systems because batteries not replaced every two years may fail, emit smoke, or catch fire. About 7,931 units were distributed worldwide.
Product
Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139, K061525, K082374, K092140, K102388, K121062). Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cepha
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0749-2023·2022-12-28
HeartWare HVAD ventricular assist pump driveline cover hardening recall
HeartWare HVAD ventricular assist pump kits may develop hardened driveline covers that impair access to critical connectors. If urgent servicing is needed, delayed access could result in patient harm from prolonged pump stoppage.
Product
HeartWare HVAD Pump Kit, REF 1205
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0742-2023·2022-12-28
HeartWare Model 1100 driveline cover hardening may delay urgent access
HeartWare Model 1100 driveline covers may harden over time, making it difficult or impossible to access the driveline-to-controller connector. A delay in accessing the connector during an urgent issue could result in prolonged pump stoppage and patient harm.
Product
HeartWare Model 1100
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0200-2023·2022-12-28
Frozen Pizza Dough Recalled for Possible Foreign Object Contamination
It'll Be Pizza is recalling 22 oz Blonde, 20 oz Blonde EZ, and 24 oz Blonde EZ frozen pizza dough due to foreign object contamination from packaging. Products were distributed in Maine, Vermont, Massachusetts, Pennsylvania, and New Hampshire.
Product
22 oz Blonde; 20 oz Blonde EZ; 24 oz Blonde EZ frozen pizza dough manufactured by It'll Be Pizza
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0730-2023·2022-12-28
GE B125P Patient Monitor CO2 Display May Show Inaccurate Readings at High Altitudes
GE is recalling B125P patient monitors because CO2 measurements may be inaccurate when used at non-sea-level altitudes in mmHg or kPa mode.
Product
B125P Patient Monitor (with E-module slot option), REF 6160000-002
Category
Medical Device
Distribution
0 states
HighFDA (Drugs)·D-0085-2023·2022-12-28
Oxcarbazepine 600mg tablets recalled for foreign substance contamination
Sun Pharmaceutical is recalling three lots of Oxcarbazepine 600mg tablets due to the presence of foreign substances. The affected medication was distributed nationwide.
Product
OXCARBAZEPINE — OXCARBAZEPINE (OXCARBAZEPINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0739-2023·2022-12-28
Abbott Alinity m Resp-4-Plex Amp Kit Recalled for False Test Results
Abbott Molecular is recalling specific lots of the Alinity m Resp-4-Plex Amp Kit due to reports of false positive and false negative test results.
Product
Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-096
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0204-2023·2022-12-28
King Oscar Anchovies Recalled for Elevated Histamine Levels
King Oscar Anchovies in Olive Oil are being recalled because they were found to contain elevated levels of histamine. The recall affects 263 cases distributed to wholesalers in Illinois and New Hampshire.
Product
King Oscar Anchovies Flat Fillet in Olive Oil 2 oz. can 18 cans per carton UPC number: 3480060061 Ingredients: Anchovies, Olive Oil, Salt. Packed in Peru Distributed by: Tri-Union Seafoods, LLC, El Segundo, CA 90245 USA
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-0732-2023·2022-12-28
GE B125M Patient Monitor CO2 Measurement Inaccuracy at High Elevations
GE B125M patient monitors may display inaccurate CO2 measurements at high elevations when using mmHg or kPa units. Measurement accuracy can be affected in locations significantly above sea level.
Product
B125M Patient Monitor, REF 6160000-004-XXXXXX
Category
Medical Device
Distribution
0 states

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20051–20075 of 27461