The Recall Desk

State

New York product recalls

73,741 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,955
Critical
1,508
Severe
3,701
Most recent
2026-10-28

Of the 12,955 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 3,701 (29%) are Severe.

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37776–37800 of 86696

  • HighCPSC·19203·2019-09-10

    DIANA Stormrider Gen 2 Air Rifles Recalled for Unexpected Discharge Risk

    DIANA is recalling Stormrider Gen 2 air rifles because they can unexpectedly discharge even when the safety is engaged, posing a risk of serious injury or death.

    Product
    DIANA® Stormrider Gen 2 Air Rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V647000·2019-09-09

    Isuzu Recalls 2017-2019 Trucks for Potential Electrical Wiring Defect

    Isuzu is recalling 2017-2019 N-Series and Chevrolet Low Cab Forward trucks because a loose bolt in the relay box may cause electrical failure and vehicle stalling.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 6500, LOW CAB FORWARD 4500, LOW CAB FORWARD 3500, N-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V648000·2019-09-09

    Mercedes-Benz Recalls 2020 GLE Models for Missing Head Restraint Manual Info

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because the owner's manuals lack instructions for adjusting third-row head restraints, violating federal safety standards.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E060000·2019-09-06

    TAP Recalls Pro Comp Lug Nuts Due to Incorrect Sizing

    TAP Worldwide is recalling 840 Pro Comp Extended Thread lug nuts that may be incorrectly sized. The defect could prevent proper tightening, leading to lug stud failure and increased crash risk.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V643000·2019-09-06

    GM Recalls 2020 Buick Enclave and Chevrolet Traverse for Frame Rail Crack

    General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V645000·2019-09-06

    GM Recalls Trucks and SUVs for Brake Vacuum Pump Defect

    General Motors is recalling 2014-2018 Chevrolet, GMC, and Cadillac vehicles because a vacuum pump defect may reduce brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, SILVERADO 1500, SIERRA 1500, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V644000·2019-09-06

    GM Recalls 2019 Chevrolet Express and GMC Savana for Seatbelt Warning Defect

    General Motors is recalling 2019 Chevrolet Express and GMC Savana vehicles because the seatbelt-unfastened warning light may fail to illuminate for five seconds after ignition.

    Product
    GMC — GMC, CHEVROLET SAVANA, EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V646000·2019-09-06

    Temsa Recalls Buses Due to Inadequate Emergency Exit Window Labels

    Temsa is recalling 2013-2020 TS35C, TS35E, and TS45 buses because emergency exit window labels may not clearly describe how to open them quickly.

    Product
    TEMSA — TEMSA TS35C, TS45, TS35E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V642000·2019-09-06

    GM Recalls 2018 Chevrolet Malibus Due to Engine Software Error

    General Motors is recalling 2018 Chevrolet Malibus with 1.5L turbo engines because a software error may disable fuel injectors, causing the engine to stall.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·090-2019·2019-09-05

    BCI Foods Recalls Meat and Poultry Soup Products Lacking Import Inspection

    BCI Foods is recalling approximately 3,304 pounds of meat and poultry soup products that were imported without the required USDA inspection.

    Product
    BCI Foods Inc. Recalls Meat and Poultry Soup Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·19202·2019-09-05

    MOMO Quick Release Steering Wheel Adapters Recalled for Crash Hazard

    MW Company is recalling MOMO Quick Release Steering Wheel Adapters for race cars because the quick release mechanism can activate inadvertently, causing the steering wheel to detach and posing a crash hazard.

    Product
    MOMO Quick Release Steering Wheel Adapters for Race Cars
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19201·2019-09-05

    STIHL PolyCut Mowing Heads Recalled Due to Injury Hazard

    STIHL is recalling about 73,000 PolyCut mowing heads because loose bolts can cause the unit to come apart, posing an injury risk.

    Product
    STIHL PolyCut ™ Mowing Heads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19779·2019-09-05

    Walker Edison Recalls Children's Bunk Beds Due to Fall Hazards

    Walker Edison Furniture is recalling about 1,200 children's bunk beds because support boards can break, posing fall and injury hazards.

    Product
    Children's bunk beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2093-2019·2019-09-04

    FDA Recalls Fresh Basil Tested Positive for Salmonella

    Harvest Sensations, LLC is recalling fresh basil that tested positive for Salmonella. The product was imported from Mexico and distributed in New York.

    Product
    Fresh basil packaged in plastic bags, each weighing one pound. (No label)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2386-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc. is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393420, 14.5F, Straight, 42cm length, BARD, UDI: 00801741012228
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-2378-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913230, 16F, Straight, 23cm length, BARD, UDI: 00801741013843
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Food)·F-2094-2019·2019-09-04

    AWERS Grained Salmon Caviar Recalled for Potential Botulism Contamination

    AWERS Inc is recalling Grained Salmon Caviar due to potential Clostridium botulinum contamination. Consumers should check their refrigerators for the specific product details.

    Product
    Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1845-2019·2019-09-04

    Pfizer Recalls Relpax Tablets Due to Microbial Contamination

    Pfizer is recalling specific lots of Relpax (eletriptan HBr) tablets because they may be contaminated with Burkholderia and Pseudomonas bacteria.

    Product
    RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2089-2019·2019-09-04

    Confectionery Arts International Recalls Jewel Dust Pearlescent Pigment

    Confectionery Arts International is recalling Jewel Dust pearlescent pigment because borosilicate glass material was found in an FDA sample.

    Product
    All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and sold prior to 4/25/19; 4g packed in 1/4 oz. jars and 14g packed in 1 oz. jars.
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Devices)·Z-2367-2019·2019-09-04

    Siemens Artis X-Ray Systems Recalled for Patient Table Cracks

    Siemens is recalling 17 Artis zee and Artis Q interventional X-ray systems because cracks in the patient table mainframe could cause the upper bed to detach, posing a hazard to patients and staff.

    Product
    Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material Number Artis zee biplane 10094141; Artis Q floor 10848280; Artis Q biplane 10848282; Artis Q.zen floor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2379-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recall for Tip Defects

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913270, 16F, Straight, 27cm length, BARD, UDI: 00801741013850
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2405-2019·2019-09-04

    Siemens SOMATOM go.Top CT Scanner Recall for Falling Injector Holder

    Siemens is recalling SOMATOM go.Top CT scanners because the injector holder could fall off with the injector and storage box.

    Product
    SOMATOM go.Top; Models #11061648 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2377-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Defect

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913190, 16F, Straight, 19cm length, BARD, UDI: 00801741013836
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2380-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 46 units of Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913350, 16F, Straight, 35cm length, BARD, UDI: 00801741013874
    Category
    Medical Device
    Distribution
    53 states