The Recall Desk

State

New York product recalls

73,824 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.

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49601–49625 of 86780

  • ModerateFDA (Drugs)·D-1041-2017·2017-08-09

    Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications

    Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.

    Product
    Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054, NDC 68382-031-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1043-2017·2017-08-09

    Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications

    Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.

    Product
    Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1057-2017·2017-08-09

    PD-Rx Pharmaceuticals Recalls Famotidine 20 mg Tablets for Weight Issues

    PD-Rx Pharmaceuticals is recalling 100 bottles of Famotidine USP 20 mg tablets because they failed to meet tablet weight specifications.

    Product
    Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2780-2017·2017-08-09

    Ortho Solutions Recalls Mislabelled Oxford AFN End Caps

    Ortho Solutions Inc is recalling 277 units of Oxford/Oxbridge AFN End Caps due to material mislabeling. The affected devices were distributed to Maryland, New York, and Pennsylvania.

    Product
    Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp 12 mm x10 mm The end caps are a circular disk with a small threaded shaft to be screwed to the distal end of the Nail.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1044-2017·2017-08-09

    Bayer Recalls Alka-Seltzer Tablets Due to Defective Blister Pack Foil

    Bayer HealthCare is recalling Alka-Seltzer Original effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.

    Product
    Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1039-2017·2017-08-09

    Teva Recalls Albuterol Sulfate Inhalation Solution Due to Impurities

    Teva Pharmaceuticals USA is recalling Albuterol Sulfate Inhalation Solution because high levels of a related compound were detected.

    Product
    Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials For Inhalation per carton, Rx only, Mfd. for: Watson Laboratories, Inc., Corona, CA 92880; Mfd. by: Cipla Ltd., Verna, Goa INDIA, NDC 0591-3467-53.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V495000·2017-08-08

    BMW Recalls 2012-2013 X3 and M6 Models for Air Bag Defect

    BMW is recalling 2012-2013 X3 and 2013 M6 vehicles because a defective driver's air bag inflator could cause metal fragments to strike occupants in a crash.

    Product
    BMW — BMW X3, M6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V496000·2017-08-08

    Dodge Charger and Challenger Recall for Engine Oil Cooler Hose Failure

    Chrysler is recalling 2017 Dodge Charger and Challenger vehicles with Hellcat engines because engine oil cooler hoses may fail, causing rapid oil loss and increased crash or fire risk.

    Product
    DODGE — DODGE CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E045000·2017-08-08

    Hickory Springs Recalls CE White Convertible School Bus Seats

    Hickory Springs is recalling CE White Convertible School Bus Seats due to inadequate padding on D-ring mounting studs, which may increase injury risk in rear-end collisions.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17203·2017-08-08

    Polaris Recalls Scrambler All-Terrain Vehicles Due to Throttle Switch Failure

    Polaris is recalling 2,800 Scrambler XP 1000 ATVs because the throttle release switch can fail, posing a crash hazard. Consumers should stop using the vehicles and contact Polaris for a free repair.

    Product
    Polaris Scrambler all-terrain vehicle (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17201·2017-08-08

    NVIDIA Recalls European Plug Heads for Power Adaptors Due to Shock Hazard

    NVIDIA is recalling European plug heads for SHIELD power adaptors because they can break and expose metal prongs, posing an electric shock hazard.

    Product
    European plug heads for NVIDIA SHIELD™ power adaptors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·089-2017·2017-08-07

    Good Food Concepts Recalls Raw Beef Products Due To E. Coli O26 Contamination

    Good Food Concepts is recalling approximately 1,290 pounds of raw beef products because they may be contaminated with E. coli O26.

    Product
    Good Food Concepts, LLC — Good Food Concepts, LLC. Recalls Beef Products Due To Possible E. Coli O26 Contamination
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·17E044000·2017-08-07

    K&N Recalls Powersports Oil Filters for Leak Risk

    K&N Engineering is recalling specific Powersports Oil Filters that may leak oil onto the rear tire or brake, increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17761·2017-08-07

    Firewood Recalls Vaporizers Due to Fire Hazard

    Firewood is recalling about 400 Firewood 4 vaporizers because an electrical short can cause the battery to catch fire. No injuries have been reported.

    Product
    Vaporizers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V491000·2017-08-04

    Jaguar Recalls One 2017 F-PACE for Fuel Pump Bolt Defect

    Jaguar is recalling one 2017 F-PACE because a fuel pump bolt may be too long, causing a fuel leak that increases fire risk.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V494000·2017-08-04

    Trail King Recalls 2012-2014 Gooseneck Trailers Due to Pivot Plate Defect

    Trail King is recalling 2012-2014 gooseneck trailers because a short pivot plate reinforcement may crack, causing the trailer deck to disconnect and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING GOOSENECK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V487000·2017-08-03

    GM Recalls 2017 Silverado and Sierra Trucks for Missing Child Seat Instructions

    General Motors is recalling 2017 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because the owner's manual may lack instructions for child restraint anchorage systems.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide