The Recall Desk

State

New York product recalls

73,817 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.

Which agencies issued them

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48401–48425 of 86773

  • ModerateFDA (Drugs)·D-0057-2018·2017-11-08

    Precision Dose Recalls Subpotent Carbamazepine Oral Suspension Unit Dose Cups

    Precision Dose Inc. is recalling Carbamazepine Oral Suspension USP unit dose cups because they tested below the required potency specifications.

    Product
    Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0055-2018·2017-11-08

    AvKARE Recalls Duloxetine Capsules Due to Slightly Elevated Phthalic Acid

    AvKARE is recalling 274 cartons of Duloxetine Delayed-release Capsules 20 mg due to slightly elevated levels of phthalic acid.

    Product
    Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2018·2017-11-08

    Teva Recalls Dutasteride and Tamsulosin HCl Capsules for Dissolution Failures

    Teva Pharmaceuticals is recalling specific lots of Dutasteride and Tamsulosin HCl capsules because they failed dissolution specifications.

    Product
    Dutasteride and Tamsulosin HCl Capsules, 0.5 mg/ 0.4 mg, packaged in a) 30-count bottle (NDC 0591-3771-30), b) 90-count bottle (NDC 0591-3771-19), Rx only, Manufactured by: Actavis Laboratories FL, Inc. Fort Lauderdale, FL 33314 USA; Distributed by: Actavis Pharma, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0082-2018·2017-11-08

    Wegmans Puff Fruit Dumplings Recalled for Undeclared Ingredients

    Wegmans is recalling Puff Fruit Dumplings because they contain undeclared FD&C Yellow 5, FD&C Yellow 6, Potassium Sorbate, and High Fructose Corn Syrup.

    Product
    033710 - Wegmans Puff Fruit Dumplings, 2 Pack, 6 oz. UPC: 0 77890 33710 3
    Category
    Food
    Distribution
    5 states
  • LowFDA (Drugs)·D-0056-2018·2017-11-08

    Sanofi Recalls Clofarabine Injection Vials Due to Incorrect Package Insert

    Sanofi-Aventis is recalling 422 vials of Clofarabine injection because the authorized generic product was packaged with the incorrect package insert for the brand name product.

    Product
    Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·18025·2017-11-07

    Norco Recalls Children's Bicycles Due to Crank Failure Hazard

    Norco Bicycles is recalling specific children's models because the cranksets can bend or break during use, posing a fall hazard.

    Product
    Children's bicycles with Samox cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V702000·2017-11-06

    Crysteel Recalls 2017 Dump Bodies for Driveshaft Detachment Risk

    Crysteel is recalling 2017 dump bodies built on Isuzu NRR-Series chassis because the driveshafts may detach from the rear universal joint, potentially causing loss of propulsion and increasing crash risk.

    Product
    CRYSTEEL — CRYSTEEL DUMP BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V699000·2017-11-06

    Forest River Recalls 2018 Puma Trailers for Incorrect Tire Placards

    Forest River is recalling 2018 Puma recreational trailers because the federal placards list incorrect tire size and pressure information, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V700000·2017-11-06

    Triumph Recalls 2016-2017 Speed Triple Motorcycles for Electrical Wiring Defect

    Triumph is recalling 2016-2017 Speed Triple S and R motorcycles because a charging system wire may rub against a bracket, potentially causing an electrical short and engine stall.

    Product
    TRIUMPH — TRIUMPH SPEED TRIPLE S, SPEED TRIPLE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V696000·2017-11-03

    Jayco Recalls 2016-2018 Jay Flight SLX Trailers Due to Fire Risk

    Jayco is recalling 2016-2018 Jay Flight SLX trailers because the battery circuit lacks overcurrent protection, increasing fire risk during electrical shorts.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V697000·2017-11-03

    Highland Ridge Recalls 2018 Light Trailers Due to Underrated Safety Chains

    Highland Ridge RV is recalling 2018 Light recreational trailers because the safety chains are rated for a lower weight than the trailer's actual capacity, increasing crash risk if detached.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW LIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V695000·2017-11-03

    Entegra Motorhomes Recalled for Missing Exterior Reflectors

    Entegra is recalling 2016-2018 Aspire, Anthem, Cornerstone, and Insignia motorhomes because they lack required reflectors, reducing visibility to other drivers.

    Product
    ENTEGRA — ENTEGRA ANTHEM, ASPIRE, INSIGNIA, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·18022·2017-11-02

    Kidde Recalls Fire Extinguishers with Plastic Handles Due to Failure to Discharge

    Kidde is recalling fire extinguishers with plastic handles and Pindicator models because they may fail to discharge or have nozzles detach. One death and 16 injuries have been reported.

    Product
    Kidde fire extinguishers with plastic handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V694000·2017-11-02

    Van-Con Recalls Dual Rear Wheel School Buses Due to Seat Barrier Defect

    Van-Con is recalling 2007-2017 Dual Rear Wheel school buses because the seat barrier behind the driver may be pinned, preventing it from deforming in a crash.

    Product
    VAN-CON — VAN-CON DUAL REAR WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V692000·2017-11-02

    Thor Motor Coach Recalls 2018 Motorhomes Due to Trailer Light Wiring Defect

    Thor Motor Coach is recalling 2018 Ace, Axis, Hurricane, Windsport, and Vegas motorhomes because trailer light wiring may be inserted incorrectly, causing lights to fail and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VEGAS, ACE, AXIS, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0031-2018·2017-11-01

    Lucky Mart Recalls Piyamping Anti-Itch Lotion Due to Incorrect Formulation

    Lucky Mart Inc. is recalling Piyamping Anti-Itch Lotion because it contains dexamethasone instead of the labeled hydrocortisone.

    Product
    PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0036-2018·2017-11-01

    365 Organic Raisin Bran Flakes Recalled for Undeclared Peanut Allergen

    Whole Foods Market Brand 365 is recalling 365 Organic Raisin Bran Flakes because peanut butter and cocoa balls were mistakenly packaged in the boxes, creating an undeclared peanut allergen risk.

    Product
    365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag, then cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0032-2018·2017-11-01

    Vitility Recalls MAN OF STEEL Capsules Containing Undeclared Sildenafil

    Vitility is recalling MAN OF STEEL capsules because FDA analysis found they contain undeclared sildenafil, an unapproved drug with unestablished safety and efficacy.

    Product
    MAN OF STEEL capsules, 3000mgs/grain, 1-count packets, Packaged for: One Drop Solutions, LLC, POB 231693, Sacramento, California 95823; [email protected]; www.manofsteelpills.com; UPC 1 0001001378 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0025-2018·2017-11-01

    Banner Pharmacy Recalls Succinylcholine Syringes Due to Sterility Concerns

    Banner Pharmacy Services is recalling 2,792 syringes of Succinylcholine 200 mg/10 mL because the product lacks assurance of sterility.

    Product
    Succinylcholine 200 mg/10 mL Syringe, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 95226, NDC 7025088801
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0035-2018·2017-11-01

    Weis Markets Recalls BLT Sandwiches Due to Undeclared Egg Allergen

    Weis Markets is recalling store-made BLT sandwiches because the mayonnaise contains undeclared egg. The recall follows a consumer complaint regarding the missing allergen label.

    Product
    Weis, Sunbury, PA; BLT Sandwich; 1 CT
    Category
    Food
    Distribution
    6 states