State

New Jersey product recalls

72,992 recalls have nationwide distribution and so reach New Jersey. 9,761 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,761
Critical: 1,249
Severe: 2,484
Most recent: 2026-09-25

Of the 9,761 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,484 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,761 recalls whose distribution notice names New Jersey specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7101–7125 of 82753

SevereFDA (Food)·F-0774-2025·2025-05-21
Bonya Black Cherry Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Black Cherry Yogurt Parfait due to undeclared almonds, which pose a risk to people with tree nut allergies. The product was distributed in NY, PA, MA, and NJ.
Product
Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1697-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas bet
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1698-2025·2025-05-21
AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall
Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.
Product
Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1763-2025·2025-05-21
LifeShield Infusion Safety Software Recalled for Drug Library Defects
ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.
Product
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0773-2025·2025-05-21
Bonya Strawberry-Banana Yogurt Parfait Recalled Due to Undeclared Almonds
Knockroe Inc is recalling Bonya Strawberry-Banana Yogurt Parfait (8oz) because the product contains undeclared almonds, which pose a risk to consumers with tree nut allergies.
Product
Bonya Strawberry-Banana Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0770-2025·2025-05-21
Bonya Pineapple Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Pineapple Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ because the product contains undeclared almonds, a common allergen that is not listed on the label.
Product
Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0768-2025·2025-05-21
Bonya Lemon Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Lemon Yogurt Parfait (8oz) because it contains undeclared almonds, a common allergen. The product was distributed to New York, Pennsylvania, Massachusetts, and New Jersey.
Product
Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-0420-2025·2025-05-21
Testosterone Cypionate Injection 200 mg/mL Recalled for Sterility Assurance
Empower Pharmacy is recalling Testosterone Cypionate Injection 200 mg/mL (Lot 202364, 8,230 vials) distributed nationwide because the manufacturer cannot assure the product's sterility. Consumers should stop using the product and consult their healthcare provider.
Product
Testosterone Cypionate Injection, 200 mg/mL, CIII, Rx Only, 5 mL Sterile Multiple-Dose Vial, Compounded by: Empower Pharmacy, 7601 N Sam Houston Pkwy W Ste 100, Houston, TX, 77064, Phone: (877) 562-8577, Compounding Date: 08/20/2024, Beyond Use by Date: 05/28/2025, Lot 202364.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1730-2025·2025-05-21
MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter
Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.
Product
MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0769-2025·2025-05-21
Bonya Raspberry Yogurt Parfait recalled for undeclared almonds
Knockroe Inc is recalling Bonya Raspberry Yogurt Parfait (8oz) because it contains undeclared almonds, which pose an allergy risk. The recall affects 6,984 units distributed to NY, PA, MA, and NJ.
Product
Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1770-2025·2025-05-21
Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal
Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Enterprise 1.5T, Model Number: 781145;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1783-2025·2025-05-21
Philips SmartPath to dStream 3.0T MRI Coil Adhesive Failure Recall
Philips is recalling SmartPath to dStream 3.0T MRI systems (Model 782145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
SmartPath to dStream for 3.0T, Model Number: 782145;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0771-2025·2025-05-21
Bonya Coconut Yogurt Parfait Recalled for Undeclared Almonds
Knockroe Inc is recalling Bonya Coconut Yogurt Parfait (8 oz) distributed to NY, PA, MA, and NJ because it contains undeclared almonds, a common allergen.
Product
Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1776-2025·2025-05-21
Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall
Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.
Product
Intera 1.5T Master/Nova, Model Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1782-2025·2025-05-21
Philips SmartPath dStream 1.5T MRI coil may create sharp edges
Philips is recalling SmartPath to dStream 1.5T MRI units (Model 782146) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, lacerations, or tissue injury to patients.
Product
SmartPath to dStream for 1.5T, Model Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0778-2025·2025-05-21
President Brand Kumquat Slices Recalled for Undeclared Sulfites
East CK Trading Inc. is recalling President Brand Kumquat Slices because they contain undeclared sulfites. Sulfites are a known allergen that can cause serious reactions in sensitive individuals.
Product
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear plastic jars with UPC 8 10077 20936 3
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1749-2025·2025-05-21
Abbott Alinity m Resp-4-Plex AMP Kit Multiplex PCR Test Recall
Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.
Product
Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, influenza A virus (flu A), influenza B virus
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V333000·2025-05-21
Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing
Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.
Product
MACK — MACK MD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2025·2025-05-21
Pruitt Occlusion Catheter Recalled Due to Incomplete Sterile Barrier Seals
LeMaitre Vascular is recalling Pruitt Occlusion Catheters (catalog numbers 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56) because some packages have incomplete sterile barrier seals, potentially compromising product sterility.
Product
Pruitt Occlusion Catheter. Catalog Numbers: 2103-36, 2103-46, 2103-56, E2103-36, E2103-46, E2103-56
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1772-2025·2025-05-21
Philips Intera 1.0T MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.0T Omni/Stellar MRI systems (37 units: 3 in US, 34 internationally) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that can cause skin injuries during patient scanning.
Product
Intera 1.0T Omni/Stellar, Model Number: 781102;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V330000·2025-05-21
Ram ProMaster rearview camera image may not display in reverse
Chrysler is recalling certain 2022-2025 Ram ProMaster vehicles because a software error in the security gateway module may prevent the rearview camera image displaying, failing FMVSS 111.
Product
RAM — RAM, BRAUN PROMASTER, RAM PROMASTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1779-2025·2025-05-21
Philips Intera 1.5T R11 MRI System Quadrature Body Coil Seal Adhesive Failure
Philips is recalling Intera 1.5T R11 MRI systems because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could contact patients and cause skin injuries.
Product
Intera 1.5T R11, Model Number: 781170;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1780-2025·2025-05-21
Philips Intera 3.0T Quasar Dual MRI Scanner Coil Seal Adhesive Failure
Philips is recalling the Intera 3.0T Quasar Dual MRI scanner (Model 781150) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 3.0T Quasar Dual, Model Number: 781150;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1773-2025·2025-05-21
Philips Intera 1.0T MRI Quadrature Body Coil Seal Failure Recall
Philips is recalling Intera 1.0T Power/Pulsar MRI systems (Model 781103) due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and injure patients during scanning.
Product
Intera 1.0T Power/Pulsar, Model Number: 781103;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1778-2025·2025-05-21
Philips Intera 1.5T MRI Scanner QBC Seal Adhesive Failure Risk
Philips is recalling the Intera 1.5T Power/Pulsar MRI scanner because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.
Product
Intera 1.5T Power/Pulsar, Model Number: 781105;
Category
Medical Device
Distribution
Distributed nationwide