State

New York product recalls

73,809 recalls have nationwide distribution and so reach New York. 12,956 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total: 12,956
Critical: 1,508
Severe: 3,702
Most recent: 2026-11-04

Of the 12,956 recalls naming New York we have scored against our rubric, 1,508 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,702 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43676–43700 of 86765

ModerateFDA (Drugs)·D-1192-2018·2018-09-26
Beaumont Bio-Med Recalls Skin Irritation Homeopathic Spray Due to CGMP Deviations
Beaumont Bio-Med is recalling Skin Irritation & Itch Response Homeopathic Formula due to manufacturing deviations that could result in possible microbial contamination.
Product
Skin Irritation & Itch Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7002-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3189-2018·2018-09-26
Siemens Artis Q X-Ray Systems Recalled for Temperature Control Defect
Siemens is recalling 429 Artis Q Interventional Fluoroscopic X-Ray Systems because a temperature control defect may cause the detector to cool down outside its designed working range.
Product
Artis Q Interventional Fluoroscopic X-Ray System, Model Numbers 10848280, 10848281, 10848282, 10848283, 10848354 & 10848355
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1198-2018·2018-09-26
Beaumont Bio-Med Recalls Colds & Flu Response Homeopathic Formula
Beaumont Bio-Med is recalling Colds & Flu Response Homeopathic Formula due to potential microbial contamination from manufacturing deviations.
Product
Colds & Flu Response Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7012-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3185-2018·2018-09-26
Polymedco PATHFAST Myoglobin II Cartridges Recalled for Leakage
Polymedco is recalling 272 PATHFAST Myoglobin II reagent cartridges due to a pinhole defect that may cause measurement bias.
Product
PATHFAST Myoglobin II reagent cartridge Catalog Number: PF1111-K PATHFAST¿ NTproBNP is a product for in-vitro diagnostic use with the in vitro diagnostic system PATHFAST¿ for the quantitative measurement of N-terminal-pro B-type Natriuretic Peptide (NT-proBNP) in heparinized…
Category
Medical Device
Distribution
8 states
ModerateFDA (Drugs)·D-1197-2018·2018-09-26
Beaumont Bio-Med Recalls Allergy & Hay Fever Relief Homeopathic Formula
Beaumont Bio-Med is recalling 124 bottles of Allergy & Hay Fever Relief Homeopathic Formula due to CGMP deviations that could result in possible microbial contamination.
Product
Allergy & Hay Fever Relief Homeopathic Formula, 2 FL. OZ. (59.2 mL) per amber glass oral spray bottle, Distributed by Beaumont Bio-Med, Inc., Waukon, IA 52172; NDC 58066-7011-7
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3184-2018·2018-09-26
Ortho-Clinical VITROS Chloride Slides Recalled for Analytical Performance Issues
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they failed to meet performance standards for urine samples.
Product
VITROS Chemistry Products Cl- Slides, Product Code 684 4471 Product Usage: VITROS Cl Slides (Product Code 684 4471) - For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Food)·F-1970-2018·2018-09-26
Stewart's Ice Cream Recalled for Incorrect Lid Packaging
Stewart's Shops Corp. is recalling 5,455 pints of Caramel Cone Crunch ice cream because some containers were packaged with the wrong lid.
Product
Stewart's Ice Cream Caramel Cone Crunch Carton, 1 pint, keep frozen, UPC: 082086444718
Category
Food
Distribution
2 states
LowFDA (Drugs)·D-1214-2018·2018-09-26
Lupin Recalls Morphine Sulfate Extended-Release Tablets Due to Impurity
Lupin Pharmaceuticals is recalling specific lots of Morphine Sulfate Extended-Release Tablets because testing found an impurity exceeding safety limits.
Product
MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3193-2018·2018-09-26
Ortho-Clinical VITROS Chemistry CREA Slides Recalled for Measurement Accuracy Issues
Ortho-Clinical Diagnostics is recalling VITROS Chemistry CREA Slides because they failed to meet accuracy standards for low-end creatinine measurements in serum and urine.
Product
VITROS Chemistry Products CREA Slides, Product Code 680 2584 Product Usage: VITROS CREA Slides (Product Code 680 2584) - For in vitro diagnostic use only. VITROS Chemistry Products CREA Slides quantitatively measure creatinine (CREA) concentration in serum, plasma, and…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3196-2018·2018-09-26
Smiths Medical Recalls Mislabeled Arterial Blood Sampling Kits
Smiths Medical ASD Inc. is recalling 29,600 Portex Pulsator Arterial Blood Sampling Kits because they were mislabeled with incorrect labels.
Product
Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile, RX. The firm name on the label is Smiths Medical ASD, Inc., Keene, NH.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1212-2018·2018-09-26
InvaGen Recalls Bupropion Hydrochloride Tablets Due to Impurity Levels
InvaGen Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride ER tablets because older batches failed impurity specifications.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V666000·2018-09-25
Kia Recalls 2017-2018 Niro Hybrids for Fire Risk
Kia is recalling 2017-2018 Niro hybrid vehicles because a faulty relay may overheat the rear seat, increasing the risk of a fire.
Product
KIA — KIA NIRO
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·18230·2018-09-25
Traeger Recalls Scout and Ranger Grills Due to Fire Hazard
Traeger Grills is recalling Scout and Ranger portable wood pellet grills because grease can leak from the drip tray, posing a fire hazard.
Product
Scout and Ranger portable wood pellet grills
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V667000·2018-09-25
Suzuki Recalls 2006 Grand Vitara for Power Steering Belt Tensioner Defect
Suzuki is recalling 2006 Grand Vitara vehicles because a plastic component in the power steering system can deteriorate, potentially causing a loss of steering assist and increasing crash risk.
Product
SUZUKI — SUZUKI GRAND VITARA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V669000·2018-09-25
Maintainer Service Mechanic Bodies Recalled for Driveshaft Interference Risk
Maintainer is recalling 2017-2018 Service Mechanic Bodies mounted on Ford F-Series Super Duty trucks because a hydraulic pump may interfere with the front axle driveshaft, potentially causing separation and increasing crash risk.
Product
MAINTAINER — MAINTAINER SERVICE/MECHANICBODY FORD
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V668000·2018-09-25
Volvo Recalls VNL Trucks Due to Fuel Line Burst Risk
Volvo is recalling 2016-2019 VNL trucks with Cummins ISX15 engines because a restricted fuel pump cooling circuit screen may cause the fuel line to burst.
Product
VOLVO — VOLVO VNL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18E093000·2018-09-25
Ioxus uStart Energy Storage Modules Recalled for Fire Risk
Ioxus is recalling uStart energy storage modules because a seal defect may allow moisture entry, potentially causing electrical shorts and fire.
Product
ELECTRICAL SYSTEM:12V/24V/48V BATTERY recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V665000·2018-09-25
Gillig Recalls 2017-2018 Low Floor Buses Due to Transmission Pressure Switch Failure
Gillig is recalling 2017-2018 Low Floor transit buses because pressure switches in the Allison hybrid drive units may fail, potentially causing a loss of drive and increasing crash risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18231·2018-09-25
Provata Recalls Activity Trackers Due to Burn Hazard
Provata Health is recalling about 30,000 promotional activity trackers because they can overheat and cause burns. Consumers should stop using the devices and contact the company for a free replacement.
Product
Provata activity trackers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·18229·2018-09-25
Desert Harvest Recalls Skin Repair Cream for Child-Resistant Closure Failure
Desert Harvest is recalling Reléveum Skin Repair Cream because the bottles do not meet child-resistant closure requirements, posing a poisoning risk to young children.
Product
Desert Harvest Reléveum Skin Repair Cream
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V658000·2018-09-24
Grand Design Recalls 2019 Travel Trailers Due to Axle Bearing Defect
Grand Design is recalling 2019 Reflection, Imagine, and Transcend travel trailers because missing inner axle bearings may cause overheating and fire.
Product
GRAND DESIGN — GRAND DESIGN TRANSCEND, REFLECTION, IMAGINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V660000·2018-09-24
Fontaine Recalls 2019 Infinity Trailers for Rear Impact Guard Defect
Fontaine Trailer Company is recalling 2019 Infinity trailers because incorrect rear impact guards may not prevent vehicles from sliding underneath during a crash.
Product
FONTAINE — FONTAINE INFINITY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V659000·2018-09-24
Winnebago Recalls 2019 Horizon RVs Due to Door Latch Defect
Winnebago is recalling 2019 Horizon vehicles because improperly adjusted door latch rods may allow the entry door to open while moving, increasing the risk of injury or a crash.
Product
WINNEBAGO — WINNEBAGO HORIZON
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V656000·2018-09-21
Kia Recalls 2018 Sorento Vehicles for Steering Column Weld Defect
Kia is recalling 2018 Sorento vehicles because an improperly welded cowl crossbar may allow the steering column to separate, increasing crash risk.
Product
KIA — KIA SORENTO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V655000·2018-09-21
GM Recalls 2016-2018 Chevrolet Express and GMC Savana for Fire Risk
General Motors is recalling 2016-2018 Chevrolet Express and GMC Savana vans due to a potential electrical short in the rear climate control module that could cause a headliner fire.
Product
CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
Category
Vehicle
Distribution
Distributed nationwide