The Recall Desk

State

New York product recalls

72,907 recalls have nationwide distribution and so reach New York. 12,902 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,902
Critical
1,501
Severe
3,133
Most recent
2026-09-09

Of the 12,902 recalls naming New York we have scored against our rubric, 1,501 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,133 (24%) are Severe.

These figures cover only the 12,902 recalls whose distribution notice names New York specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

876–900 of 85809

  • ModerateFDA (Food)·H-1146-2026·2026-07-15

    Wise Onion Rings recalled for undeclared food color additives

    Wise Foods Inc is recalling Wise Onion Rings, 3.75 oz packages, because they contain undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3 food colorings that are not listed on the label.

    Product
    Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-2696-2026·2026-07-15

    Medline Convenience Kits containing temperature probes recalled

    Medline Industries is recalling Convenience Kits containing Covidien Mon-a-Therm General Purpose Temperature Probes due to an error in distribution control. The recall affects 75 kits distributed nationwide.

    Product
    Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2677-2026·2026-07-15

    Aquacel Ag Surgical SP Surgical Dressing Recalled for Out-of-Specification Thickness

    ConvaTec is recalling Aquacel Ag Surgical SP dressings (Lot 5G00809) that were manufactured with greater-than-specified thickness. The dressing is used in surgical wound care.

    Product
    Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2676-2026·2026-07-15

    Olympus Single Use Distal Cover MAJ-2315 Duodenovideoscope Replacement

    Olympus Corporation of the Americas is replacing the previous design of its Single Use Distal Cover (MAJ-2315) with a newly designed version for use with EVIS EXERA III Duodenovideoscopes.

    Product
    Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flex
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0668-2026·2026-07-15

    Drogueria San Juan Isopropyl Alcohol 70% Recalled for Subpotency

    Gasco Industrial Corp. is recalling Drogueria San Juan Puerto Rico Isopropyl Alcohol 70% (1 gallon) due to subpotency. The affected lots are 250221A5 and 250224A2 distributed nationwide.

    Product
    Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 1 gallon (3.78 liter), Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana LLana Rio Piedras, PR 00924
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0667-2026·2026-07-15

    Gasco Isopropyl Alcohol 70% recalled for subpotent drug content

    Gasco Industrial Corp. is recalling Gasco Isopropyl Alcohol 70% (32 oz bottles, Lot 250218B3) distributed nationwide because the product is subpotent—containing less active ingredient than labeled.

    Product
    Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2717-2026·2026-07-15

    Versius Surgical System Console affected by cybersecurity vulnerability

    CMR Surgical Limited is recalling the Versius Surgeon Console (Model V-SS-1020, Software Version Pratchett 1 version 62.1) due to Secure Boot not being enabled at manufacturing, presenting a potential cybersecurity risk.

    Product
    Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2695-2026·2026-07-15

    Medline Anesthesia Kit Peds Contains Defective Temperature Probes

    Medline Industries is recalling Anesthesia Kit Peds (Model DYNJAP10125A, Lot 24JBR072) nationwide because they contain Covidien Mon-a-Therm temperature probes affected by a distribution control error.

    Product
    Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2701-2026·2026-07-15

    EMPOWR 3D KNEE insertion instruments recalled for incorrect product size packaging

    Encore Medical is recalling EMPOWR 3D KNEE insertion instruments because some packages contain incorrect product sizes due to a packaging discrepancy.

    Product
    Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-2713-2026·2026-07-15

    GSP Neonatal GALT Kit in vitro diagnostic test equipment

    WALLAC OY is recalling GSP Neonatal GALT Kit units due to reduced on-board stability that may increase run-QC failures and delay patient test results.

    Product
    GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0666-2026·2026-07-15

    Gasco Isopropyl Alcohol 70% recalled nationwide for subpotency

    Gasco Industrial Corp. is recalling Gasco Isopropyl Alcohol 70% (1 US Gallon) nationwide due to subpotency. The voluntary recall affects specific lot numbers manufactured before the expiration date.

    Product
    Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon (3.78 L), Manufactured by: Gasco Industrial Corp., PO Box 1360, Gurabo, PR 00778, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2702-2026·2026-07-15

    5008X Blood Tubing Set connection errors FDA Class II recall

    Fresenius Medical Care is recalling 5008X Blood Tubing Sets due to potential online port errors that may occur when connecting the SafeLine to the substitution fluid port of the 5008X CAREsystem.

    Product
    5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF St
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E046000·2026-07-14

    Ford Recalls Integrated Trailer Brake Control Kits for F-150s

    Ford is recalling specific integrated trailer module accessory kits for 2021-2026 F-150s because they may lose communication, causing a loss of trailer brakes and lights.

    Product
    EXTERIOR LIGHTING:TAIL LIGHTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V450000·2026-07-14

    Winnebago Recalls 2027 Navion and View RVs for Fire Risk

    Winnebago is recalling 2027 Navion and View recreational vehicles because a rooftop fan circuit board may overheat and cause a fire.

    Product
    WINNEBAGO — WINNEBAGO NAVION, VIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V452000·2026-07-14

    2026 Hyundai Kona rear center seat belt buckle failure risk

    Hyundai is recalling certain 2025 Kona Electric and 2026 Kona vehicles because the rear center seat belt buckle may fail to properly restrain an occupant during a crash. Dealers will replace the buckle assembly for free.

    Product
    HYUNDAI — HYUNDAI KONA, KONA ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E045000·2026-07-10

    Tenneco Recalls NAPA Steering Inner Tie Rod Ends for Ford Vehicles

    Tenneco Automotive is recalling NAPA steering inner tie rod ends for certain Ford C-Max, Escape, and Focus models because the stud may separate, causing a loss of steering.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V446000·2026-07-10

    Grand Design Lineage RVs Recalled for Rooftop Fan Fire Risk

    Grand Design is recalling 2026-2027 Lineage RVs because a rooftop fan component may overheat and cause a fire. Dealers will replace the part free of charge.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26608·2026-07-09

    Moodooy Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

    Moodooy Adult Portable Bed Rails sold on Amazon violate mandatory safety standards and pose risk of entrapment and asphyxiation. The rails lack required warning labels and users can become trapped within the rail or between the rail and mattress.

    Product
    Moodooy Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26610·2026-07-09

    Flaunt MagSafe Battery Chargers Recalled for Fire and Burn Hazards

    About 1,400 Flaunt MagSafe Battery Chargers (model E33A) are being recalled because the lithium-ion battery can overheat and ignite. The company has received five reports of the power banks catching fire, including two reports of burns and four reports of property damage.

    Product
    Flaunt MagSafe Battery Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V444000·2026-07-09

    2026 Volvo VNL, VNR, VHD, VN, VAH trucks recalled for loose steering

    Volvo Trucks is recalling certain 2026 VNL, VNR, VHD, VN, and VAH vehicles because the steering arm may not be tightly fastened to the steering knuckle, risking loss of steering control and crashes.

    Product
    VOLVO — VOLVO VNL (4), VNR (4), VN, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide