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.

776–800 of 85809

  • HighNHTSA·26E047000·2026-07-22

    Hiab Recalls K-HiPro Cranes Due to Potential Column Weld Failure

    Hiab USA Inc. is recalling K-HiPro 425 and 505 cranes because a weld may crack, risking column collapse and injury.

    Product
    EQUIPMENT:MECHANICAL:BOOM/CRANE/LADDER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2719-2026·2026-07-22

    Olympus Toomey Evacuator 50cc with Adaptor sterilization recall

    Olympus is recalling the Toomey Evacuator 50cc with Adaptor (Model 188A) because some sterilization parameters in the instructions may not reliably render the devices sterile.

    Product
    Olympus Toomey Evacuator 50cc with Adaptor. Model Number: 188A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1155-2026·2026-07-22

    Pillsbury Kaiser Roll Dough recalled for potential glass contamination

    General Mills is recalling Pillsbury Bread Rolls, Kaiser Roll Dough due to potential foreign glass material in the product. Affected consumers should not consume the product and should contact the company or retailer for a refund.

    Product
    Pillsbury Bread Rolls, Kaiser Roll Dough. 144 units / 2.5oz each. Net Wt. 22.5 lb (10.2kg) Package UPC 7 21582-13288 9. Case UPC 107-21582-13288-6. Keep Frozen. Case Qty 144. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
    Category
    Food
    Distribution
    19 states
  • HighNHTSA·26V471000·2026-07-22

    ATC Recalls 2026 RM500 and RM700 Trailers Due to Winch Remote Issue

    Aluminum Trailer Company is recalling 2026 RM500 and RM700 trailers because the wireless remote may cause unexpected winch movements, increasing injury risk.

    Product
    ATC — ATC RM700, RM500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1154-2026·2026-07-22

    Pillsbury Bread Rolls Hard Roll Dough Recalled for Glass

    General Mills is recalling Pillsbury Bread Rolls Hard Roll Dough due to potential glass contamination. Affected products were distributed across multiple states.

    Product
    Pillsbury Bread Rolls, Hard Roll Dough. 180 units / 2.25oz each. Net Wt. 25.31 lb (11.48kg) Package UPC 721582-13283 4. Case UPC 107-21582-13283-1. Keep Frozen. Case Qty 180. Distributed by: General Mills Sales, Inc. Minneapolis, MN 55440.
    Category
    Food
    Distribution
    19 states
  • HighFDA (Devices)·Z-2738-2026·2026-07-22

    Medtronic DLP One-Piece Pediatric Arterial Cannula Recalled for Foreign Material

    Medtronic is recalling certain DLP One-Piece Pediatric Arterial Cannulas (Product Number 77010) due to complaints of loose foreign material containing trace levels of blood found in the devices.

    Product
    Medtronic DLP One-Piece Pediatric Arterial Cannula, Product Number/CFN 77010; Cardiopulmonary bypass vascular cannula
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1165-2026·2026-07-22

    Ice Pop D'Dioses Pistachio Recalled for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Pistachio Ice Pop (1 Bar, 81.7 g) because it may contain undeclared milk, pecans, pistachios, yellow #5, and red #40.

    Product
    Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2721-2026·2026-07-22

    Olympus Glass Body for 194 Ellik Evacuator Model 190A Sterilization Recall

    Olympus Corporation is recalling the Glass Body for 194 Ellik Evacuator (Model 190A) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.

    Product
    Olympus Glass Body for 194 Ellik Evacuator. Model Number: 190A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1164-2026·2026-07-22

    Ice Pop D'Dioses Rompope recalled for undeclared allergens

    D'Dioses Rompope ice pops may contain undeclared milk, pecans, pistachios, and food color additives (yellow #5 and red #40). The product was distributed in NJ, CT, NY, and PA.

    Product
    Ice Pop, D'Dioses Rompope, 4 oz (85 g), with UPC 710594511812
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·26V473000·2026-07-22

    2024–2026 Volkswagen Atlas and Atlas Cross Sport Rearview Camera Software

    Volkswagen is recalling 2024–2026 Atlas and Atlas Cross Sport vehicles due to a low-voltage electrical event that may cause the rearview camera display to fail, reducing rear visibility.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2741-2026·2026-07-22

    Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall

    Maquet Cardiovascular is recalling Vasoview Hemopro 2 devices from Lot 3000547797 due to exposure to out-of-specification sterilization during gamma sterilization. The affected devices may not be properly sterilized.

    Product
    The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000; UDI 00607567700406) is a sterile, single-use Class II device that was cleared for marketing by FDA under 510(k) number K101274.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1172-2026·2026-07-22

    Ice Pop D'Dioses Tamarindo Recalled for Undeclared Allergens

    D'Dioses Tamarindo ice pops may contain undeclared milk, pecans, pistachios, yellow #5, and red #40. Consumers with allergies to these ingredients should not consume the product.

    Product
    Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·26V472000·2026-07-22

    Coach and Equipment Recalls Phoenix and Metrolite Buses with Lift Defect

    Coach and Equipment is recalling 2024-2026 Phoenix and Metrolite buses because a wheelchair lift may fail to stop, increasing injury risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METROLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2730-2026·2026-07-22

    Orthofix MINIRAIL external fixation devices recalled for incorrect labeling

    Orthofix U.S. LLC is recalling 19 units of Orthofix MINIRAIL orthopedic external fixation devices distributed across the US due to incorrect model labeling that could lead to surgical use of the wrong device.

    Product
    Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma external fixation device
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-2725-2026·2026-07-22

    Rapid Refill Continuous Injection System Recalled for Syringe Loosening Risk

    Boston Scientific's Rapid Refill Continuous Injection System (UPN M00566001) is being recalled because the recalled Medline Namic Angiographic Control Syringe may loosen or disconnect from the manifold, potentially causing leakage, inability to aspirate or inject, and procedure delays.

    Product
    Rapid Refill Continuous Injection System, UPN M00566001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2026·2026-07-22

    GE Optima XR200/220/240amx Radiographic System Column Safety Mechanism

    GE Medical Systems is recalling certain Optima XR200/220/240amx mobile radiographic systems after column replacements because functional testing of the safety pawl may not have been performed, which could allow the X-ray arm to drop and injure patients.

    Product
    Optima XR220amx, Mobile Digital-Ready Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2728-2026·2026-07-22

    Mobile Digital Radiographic System Arm Drop Risk During Patient Exams

    GE HealthCare is recalling certain Optima XR200/220/240amx Mobile Digital Radiographic Systems due to potential failure of the Column Safety mechanism, which could cause the X-ray arm to drop during patient exams. The issue stems from incomplete functional testing of the safety pawl after column replacement.

    Product
    Optima XR240amx, Mobile Digital Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V475000·2026-07-22

    Freightliner Trucks Recalled for Low Beam Headlight Software Error

    Daimler Trucks North America is recalling 2026-2027 Freightliner models because a software error may cause low beam headlights to illuminate improperly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC EM2, BUSINESS CLASS M2, S2RV, S2C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1168-2026·2026-07-22

    D'Dioses Pina Colada Ice Pop Bar Recall for Undeclared Allergens

    D'Dioses Fruit Pops, Inc. is recalling D'Dioses Pina Colada ice pop bars because they may contain undeclared milk, pecans, pistachios, yellow #5, and red #40 dyes.

    Product
    Ice Pop, D'Dioses Pina Colada, 1 Bar (81.7 g), with UPC 710594511225
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2718-2026·2026-07-22

    Olympus Toomey Evacuator 30cc medical device sterilization parameters recalled

    Olympus Corporation recalled the Toomey Evacuator 30cc with Adaptor (Model 188) because certain sterilization parameters in the instructions may not consistently render the devices adequately sterile.

    Product
    Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2734-2026·2026-07-22

    Papablic Replacement Brush Heads Recalled Due to Breakage Risk

    Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.

    Product
    Papablic Replacement Brush Heads. Model Number: PAPA317AA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2731-2026·2026-07-22

    Orthofix Articulated Minirail Fixator devices recalled for incorrect labeling

    Orthofix U.S. LLC is recalling Articulated Minirail Fixator external fixation devices due to incorrect model labeling. Three models were mislabeled: M101 labeled as M103, M103 labeled as M101, and M122 labeled as M111.

    Product
    Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral orthopedic/trauma external fixation device
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-0679-2026·2026-07-22

    Clinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide

    Bell Pharmaceuticals is recalling Clinere Ear Wax Remover nationwide because the product contains significantly reduced active ingredient and low pH. The affected lots were distributed throughout the United States.

    Product
    CLINERE EAR WAX REMOVER — CLINERE EAR WAX REMOVER (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0680-2026·2026-07-22

    Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall

    Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.

    Product
    QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1174-2026·2026-07-22

    Amy's Organic Lentil Soup Recalled for Potential Spoilage Risk

    Amy's Kitchen is recalling Amy's Organic Soups Lentil Light in Sodium (14.5 oz cans) due to potential for spoilage. The recall affects approximately 15,350 cases distributed across multiple U.S. states and Canada.

    Product
    Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl. Cover. Cook for 1.5-2 minutes. Let sit 1 minute. Stir. Serve. Stovetop: Heat soup in a saucepan, stirring occasionally. AMY'S KITCHEN, INC. P.O. BOX 7129 PETAL
    Category
    Food
    Distribution
    28 states