The Recall Desk

State

New York product recalls

73,388 recalls have nationwide distribution and so reach New York. 12,941 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,941
Critical
1,511
Severe
3,698
Most recent
2026-10-07

Of the 12,941 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.

These figures cover only the 12,941 recalls whose distribution notice names New York specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21751–21775 of 86329

  • HighFDA (Devices)·Z-0009-2023·2022-10-12

    Introcan Safety Catheter Recalled for Potential Leakage at Hub

    B. Braun is recalling 94,000 Introcan Safety FEP 14G catheters due to potential leakage at the catheter hub. Affected units were distributed in the US and Canada.

    Product
    Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-0005-2023·2022-10-12

    Wright Medical EVOLVE Proline Stem Labeling Error Recall

    Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.

    Product
    stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1858-2022·2022-10-12

    Hologic BioZorb LP Implant Markers Recalled Due to Mislabeled Expiration Date

    Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.

    Product
    The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The BioZorb LP Marker is comprised of a bioabsorbable PLA (polylactic acid) component which resorbs completely in 1 year or more and a permanent component…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0002-2023·2022-10-12

    Whole Foods Organic Caesar Dressing Recalled for Undeclared Wheat and Soy

    WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.

    Product
    WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market: Austin, TX Expanded recall to include the best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0008-2023·2022-10-12

    Hammertoe Continuous Compression Implant Kit Drill Pin Incompatibility

    Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.

    Product
    Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V764000·2022-10-12

    2022 Volkswagen ID.4 Rearview Camera May Be Delayed or Deactivated

    2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0003-2023·2022-10-12

    Aurora Natural Organic Cranberry Mix recalled for undeclared peanuts

    Aurora Products is recalling its Aurora Natural brand Organic Cranberry Frontier Mix due to undeclared peanuts. People with peanut allergies are at risk.

    Product
    Aurora Natural brand; Organic Cranberry Frontier Mix UPC: 6 55852 00730 3; 19 oz (538g); Ingredients: ORGANIC DRIED CRANBERRIES (ORGANIC CANE SUGAR, ORGANIC SUNFLOWER OIL), ORGANIC RAISINS, ORGANIC DATES (ORGANIC OAT COVERING), ORGANIC CASHEWS, ORGANIC PEPITAS, ORGANIC ALMONDS.…
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-0030-2023·2022-10-12

    Herbal Dietary Supplement Recalled for High Bacterial Growth

    Eden's Answers Inc is recalling Sprigs Dental Health, an herbal dietary supplement, due to detection of high bacterial growth. The product was distributed across 37 states.

    Product
    Sprigs - Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·F-0031-2023·2022-10-12

    Herbal Dietary Supplement Sprigs Honey Herbal Syrup Recalled for Bacterial Growth

    Eden's Answers Inc is recalling Sprigs Honey Herbal Syrup dietary supplement due to high bacterial growth within the product. The affected product was distributed across multiple states.

    Product
    Sprigs - Honey Herbal Syrup: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Drugs)·D-0007-2023·2022-10-12

    Phytonadione Injectable Emulsion recalled for failed stability testing

    Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.

    Product
    PHYTONADIONE — PHYTONADIONE (PHYTONADIONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1551-2022·2022-10-12

    Tranexamic Acid Injection Recalled for Metal Particulate Matter

    AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.

    Product
    TRANEXAMIC ACID — TRANEXAMIC ACID (TRANEXAMIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V759000·2022-10-11

    FCA Recalls 2019-2020 Ram 4500 and 5500 for Brake Hose Defect

    FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.

    Product
    RAM — RAM 4500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V760000·2022-10-11

    Kia K5 Transmission Malfunction May Cause Complete Loss of Drive Power

    Kia is recalling certain 2021-2023 K5 and 2021-2022 Sorento vehicles with transmission oil pump malfunction that may cause complete loss of drive power, increasing crash risk.

    Product
    KIA — KIA K5, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V761000·2022-10-11

    Alamo Recalls 2021-2022 Schwarze A9SE Monsoon Street Sweepers

    Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.

    Product
    SCHWARZE — SCHWARZE A9SE MONSOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E086000·2022-10-11

    Chrysler Recalls Mopar Brake Hoses Due to Rupture Risk

    Chrysler is recalling specific Mopar brake hoses because the inside diameter may be too small, causing rupture and loss of braking ability.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V758000·2022-10-10

    Wabash National Recalls 2020-2023 RFALHSA Trailers for Visibility Defect

    Wabash National is recalling 2020-2023 RFALHSA trailers because the lift gate obscures rear conspicuity tape, reducing visibility and increasing crash risk.

    Product
    WABASH NATIONAL — WABASH NATIONAL RFALHSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V757000·2022-10-10

    Fontaine Recalls 2020-2023 Elgin Sweepers Due to Air Line Defect

    Fontaine is recalling 56 Elgin sweepers because a braided air line may rub through an oil tube, causing pump failure and loss of power.

    Product
    ELGIN SWEEPER — ELGIN SWEEPER CROSSWIND 1 (PB 220)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V755000·2022-10-08

    Riverside Recalls 2023 Travel Trailers Due to Awning Seam Defect

    Riverside RV is recalling 2023 Retro, Intrepid, and Xplorer travel trailers because a welded seam on the electric awning may separate, posing an injury risk.

    Product
    RIVERSIDE — RIVERSIDE XPLORER, INTREPID, RETRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V753000·2022-10-07

    Volkswagen Atlas Engine Bearing Defect Recall 2022 through 2023

    Volkswagen is recalling 2022 and 2023 Atlas and Cross Sport vehicles because engine connecting rod bearings may become damaged, causing engine failure and stalling. This increases crash and fire risk.

    Product
    AUDI — AUDI, VOLKSWAGEN Q5 SPORTBACK, Q5, ATLAS CROSS SPORT, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V748000·2022-10-07

    2023 Newmar Dutch Star Motorhome Brake Pedal Contact May Cause Brake Failure

    Newmar is recalling certain 2023 Dutch Star motorhomes because the brake pedal may contact the dash panel, causing unintended brake engagement. This can lead to brake failure and increase crash risk.

    Product
    NEWMAR — NEWMAR DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V752000·2022-10-07

    2022 BMW motorcycles recalled for improperly lubricated clutch cover bolts

    BMW is recalling certain 2022 and 2023 motorcycles with improperly lubricated clutch cover bolts that may loosen and cause oil leaks, increasing crash and fire risks. Free bolt replacement is available through BMW dealers.

    Product
    BMW — BMW S 1000 R, S 1000 XR, M 1000 RR, S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V749000·2022-10-07

    Newmar Recalls 2020-2023 Super Star Motorhomes for Incorrect Tire Labeling

    Newmar is recalling 2020-2023 Super Star motorhomes because the Federal Certification label may list incorrect rear tire sizes, potentially leading to improper tire installation.

    Product
    NEWMAR — NEWMAR SUPER STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide