The Recall Desk

State

New York product recalls

72,992 recalls have nationwide distribution and so reach New York. 12,906 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,906
Critical
1,501
Severe
3,136
Most recent
2026-09-25

Of the 12,906 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 3,136 (24%) are Severe.

These figures cover only the 12,906 recalls whose distribution notice names New York specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7976–8000 of 85898

  • HighCPSC·25184·2025-03-20

    Adjustable Dumbbells Recalled for Weight Plate Dislodging Impact Hazard

    Weight plates on FitRx SmartBell XL dumbbells can dislodge during use, causing impact injuries. More than 60 incidents reported, linked to 7 documented injuries including bruises and contusions.

    Product
    FitRx SmartBell XL Quick-Select 10-90 lbs. Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25194·2025-03-20

    Benadryl Liquid Elixir 100 mL bottles lack child-resistant packaging

    Arsell is recalling Benadryl Liquid Elixir 100 mL bottles sold on Amazon because the packaging is not child-resistant as required by federal law. The medication could poison children if ingested.

    Product
    Benadryl Liquid Elixir, 100 mL bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·25190·2025-03-20

    Wireless portable power banks recalled due to fire and burn hazards

    VC Group recalls 89,500 MagSafe wireless power banks because lithium-ion batteries can overheat and ignite. The company received 19 fire reports resulting in 10 minor injuries.

    Product
    VC Group MagSafe Wireless Power Pack Portable Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25189·2025-03-20

    Woolite Delicates Detergent Recalled Due to Bacterial Contamination Risk

    Reckitt is recalling approximately 16,200 bottles of Woolite Delicates detergent sold exclusively on Amazon due to potential Pseudomonas bacteria contamination. The bacteria poses a serious infection risk to people with weakened immune systems or external medical devices.

    Product
    Woolite Delicates detergent in 50-fluid-ounce bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25192·2025-03-20

    GIKPAL 10 Drawer Dressers Recalled for Tip-Over and Entrapment Risk to Children

    GIKPAL 10 Drawer Dressers sold on Walmart.com are recalled for tip-over and entrapment hazards to children if not anchored to a wall. About 28,590 units were sold between September 2023 and January 2025.

    Product
    GIKPAL 10 Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V176000·2025-03-20

    IC school bus low beams turn off with high beams

    International is recalling certain 2025-2026 IC Bus CESB school buses with halogen headlights because activating the high beams turns the low beams off, failing FMVSS 108.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V175000·2025-03-20

    GM Recalls 2016-2018 Cadillac and Chevrolet Vehicles for Steering Defect

    General Motors is recalling specific 2016-2018 Cadillac and Chevrolet vehicles because the electric power steering assist may fail, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET CTS, ATS, CORVETTE, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V174000·2025-03-20

    Jeep Wagoneer S headlights cannot be aimed properly

    Chrysler is recalling certain 2024-2025 Jeep Wagoneer S electric vehicles because the headlight vertical aim adjustment is not accessible and the horizontal aim is not covered, failing FMVSS 108.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V171000·2025-03-20

    Thor Motor Coach motorhomes slide-out room unexpected deployment risk

    Thor Motor Coach is recalling certain 2023–2026 motorhomes because the slide-out room can extend while the vehicle is moving, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM TRAVELER, FREEDOM ELITE, AXIS, VEGAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·008-2025·2025-03-20

    Idaho Smokehouse Recalls Beef Sticks Due to Possible Metal Contamination

    Idaho Smokehouse Partners is recalling approximately 29,541 pounds of Chomps Original Beef Stick Mild products due to possible metal contamination. Consumers are advised not to consume the affected items.

    Product
    Idaho Smokehouse Partners LLC — Idaho Smokehouse Partners Recalls Ready-To-Eat Beef Stick Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0633-2025·2025-03-19

    Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg

    ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.

    Product
    Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0609-2025·2025-03-19

    Aleppo Tahini Sesame Paste recalled due to Salmonella contamination

    Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.

    Product
    Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Devices)·Z-1289-2025·2025-03-19

    Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter

    Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.

    Product
    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1306-2025·2025-03-19

    Aortic Root Cannula Recall for Loose Male Luer Component

    Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.

    Product
    Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG, m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E020000·2025-03-19

    ZF Recalls Lemförder and TRW Track Control Arms for Subframe Cracking Risk

    ZF North America is recalling specific Lemförder and TRW track control arms because a short bushing sleeve may crack the subframe, potentially causing loss of vehicle control.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1304-2025·2025-03-19

    BD Alaris Systems Manager Infusion Software Affected by Programming Request Issue

    BD Alaris Systems Manager software may transmit outdated automated programming requests to progressive care units. The FDA has classified this as a Class I recall.

    Product
    BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Drugs)·D-0272-2025·2025-03-19

    Injectable Phenylephrine Solution Recalled Due to Particulate Matter Contamination

    The FDA is recalling phenylephrine injection solution due to particulate matter contamination. Three lot numbers distributed nationwide are affected.

    Product
    PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0631-2025·2025-03-19

    Ulker Rulokat hazelnut wafers recalled nationwide for undeclared egg allergen

    Ulker Rulokat Hazelnut Wafers are being recalled due to undeclared egg. The product was distributed to retail stores across Canada and 35 US states.

    Product
    Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
    Category
    Food
    Distribution
    36 states
  • SevereNHTSA·25V173000·2025-03-19

    Nissan and INFINITI front brake calipers may break losing braking

    Nissan is recalling certain 2025 Murano, Pathfinder and INFINITI QX60 vehicles because one or both front brake caliper assemblies may have reduced strength and could break, failing FMVSS 135.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2025·2025-03-19

    Potassium Chloride Injection Strength Mislabeled on Packaging Overwrap

    ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1305-2025·2025-03-19

    BD Care Coordination Engine Software May Send Outdated Programming Requests

    BD Care Coordination Engine infusion software may send outdated automated programming requests to care units. Healthcare facilities in affected US states should review their systems.

    Product
    BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Drugs)·D-0259-2025·2025-03-19

    ChloraPrep One-Step Topical Drug Recalled for Fungal Contamination

    CareFusion 213, LLC is recalling ChloraPrep One-Step, a preoperative skin preparation drug, due to non-sterility from a package lidding breach allowing fungal contamination. The recall affects 205,440 applicators distributed nationwide and in Canada.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide