The Recall Desk

State

New York product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53226–53250 of 86789

  • CriticalFDA (Food)·F-1146-2017·2017-01-11

    FDA Recalls Unbranded Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of unbranded herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204857 ** HERRING NORWAY SUPER JUMBO BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1144-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204250 ** HERRING ISLANDSKAYA JUMBO BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1155-2017·2017-01-11

    FDA Recalls Fresh Seafood Holland Herring for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 1,351 containers of Fresh Seafood Holland Herring in Oil due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Holland Herring in Oil sold under the FRESH SEAFOOD label, packaged in a plastic retail container (tub), Net Wt. 24 oz. (680g) - UPC 825512 008128 --- Produced By: R.S.B. New York, NY 11691
    Category
    Food
    Distribution
    7 states
  • CriticalCPSC·17067·2017-01-11

    Bad Boy Off-Road Utility Vehicles Recalled Due to Missing Seat Belts

    Textron Specialized Vehicles is recalling about 1,100 Bad Boy off-road utility vehicles because they lack seat belts, posing a risk of serious injury or death.

    Product
    Bad Boy off-road utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1157-2017·2017-01-11

    FDA Recalls Fresh Seafood Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling refrigerated herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine sold under the FRESH SEAFOOD label, packaged in a plastic retail container (tub), Net Wt. 46 oz. (1275g) - UPC 825512 008173 --- Produced By: R.S.B New York, NY 11691
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1145-2017·2017-01-11

    FDA Recalls Ready-to-Eat Herring in Brine Due to Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part ** 204311 ** HERRING SUPER DUNAYSKAYA BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1147-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine Due to Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of refrigerated, ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204744 ** HERRING MALOSOLNAYA (20 in barrel) ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1148-2017·2017-01-11

    FDA Recalls Bulk Herring in Brine for Listeria Risk

    Royal Seafood Baza, Inc. is recalling 405 bulk buckets of refrigerated, ready-to-eat herring in brine due to potential Listeria monocytogenes contamination.

    Product
    Refrigerated, Ready to Eat Herring in Brine with no brand name, packaged in bulk 25 lb. white plastic bucket and labeled in part, ** 204883 ** HERRING DUNAYSKAYA BY PC ** (label on the metal handle of bucket)
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-0908-2017·2017-01-11

    House of Flavors Recalls Peanut Butter Ice Cream for Listeria Risk

    House of Flavors, Inc. is voluntarily recalling Ashby's Sterling Peanut Butter Landslide Ice Cream because a supplier recalled peanut butter cookie dough potentially contaminated with Listeria monocytogenes.

    Product
    Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Drugs)·D-0366-2017·2017-01-11

    Wells Pharmacy Recalls Methylcobalamin Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 265 vials of compounded Methylcobalamin 5,000 mcg/mL Injectable because the product lacks assurance of sterility.

    Product
    Methylcobalamin 5,000 mcg/mL Injectable, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0345-2017·2017-01-11

    Wells Pharmacy Recalls Ceftazidime Ophthalmic Kits Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 46 kits of compounded Ceftazidime Ophthalmic 2.25% due to a lack of assurance of sterility.

    Product
    Ceftazidime, Lyophilized, Ophthalmic 2.25% Kit, Rx only, Compounded by Wells Pharmacy, Ocala , FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0320-2017·2017-01-11

    Tri-Coast Pharmacy Recalls TriMix Injection Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2 units of TriMix injection because the agency cannot assure the products are sterile.

    Product
    TriMix, Alprostadil/Phentolamine/Papaverine 100mcg/3mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Tyrosine Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 50 vials of compounded L-Tyrosine 10 mg/mL because the products lack assurance of sterility.

    Product
    L-Tyrosine 10 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0421-2017·2017-01-11

    Wells Pharmacy Recalls Vitamin D3 Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 335 vials of Vitamin D3 in Sesame Oil Injectable due to a lack of assurance of sterility.

    Product
    Vitamin D3 in Sesame Oil Injectable 50,000 IU/mL, 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0294-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin GT Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 920 vials of compounded Sermorelin GT nationwide due to a lack of assurance of sterility.

    Product
    Sermorelin GT (Sermorelin Acetate 15 mg/GHRP-2 5.4 mg/Theanine (L) 75 mg). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Arginine HCL Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 41 vials of compounded L-Arginine HCL 100 mg/mL because there is a lack of assurance of sterility. The products were distributed nationwide.

    Product
    L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0287-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin Acetate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 260 vials of Sermorelin Acetate 6 mg compounded between May and November 2016 because the agency cannot assure the products are sterile.

    Product
    Sermorelin Acetate 6 mg. Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0418-2017·2017-01-11

    Wells Pharmacy Recalls Trimix Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling specific vials of Trimix Injectable because the agency could not ensure the product was sterile.

    Product
    Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Testosterone Cypionate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2,818 vials of compounded Testosterone Cypionate in Grapeseed nationwide due to a lack of assurance of sterility.

    Product
    Testosterone Cypionate in Grapeseed, 200 mg/mL, (5 ML and 10 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0376-2017·2017-01-11

    Wells Pharmacy Recalls Compounded Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling MIC+B12(M)+Carnitine injectable vials due to a lack of assurance of sterility. The recall covers 159 vials distributed nationwide.

    Product
    MIC+B12(M)+Carnitine 12.5 mg/50 mg/100 mg/1 mg/50 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V032000·2017-01-11

    Audi Recalls Vehicles Due to Passenger Air Bag Inflator Rupture Risk

    Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.

    Product
    AUDI — AUDI A4, A6, S6, S4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0416-2017·2017-01-11

    Wells Pharmacy Recalls Trimix Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling Trimix Injectable vials nationwide due to a lack of assurance of sterility.

    Product
    Trimix Injectable 30 mg/1 mg/25 mcg/mL, 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0361-2017·2017-01-11

    Wells Pharmacy Recalls Glutathione Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 148 vials of Glutathione 200 mg/mL Injectable nationwide due to a lack of assurance of sterility.

    Product
    Glutathione 200 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide