The Recall Desk

State

New York product recalls

73,806 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.

These figures cover only the 12,956 recalls whose distribution notice names New York specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40651–40675 of 86762

  • SevereFDA (Food)·F-1204-2019·2019-04-03

    Bauer's Candies Recalls Salted Combo Modjeskas Due to Hepatitis A Risk

    Bauer's Candies, Inc. is recalling 1 lb salted combo modjeskas due to a risk of Hepatitis A exposure. The product was distributed to retail locations in Kentucky and Illinois, and to private individuals in multiple states and Iceland.

    Product
    1 lb salted combo modjeskas
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1202-2019·2019-04-03

    Bauer's Candies Recalls Salted Combo Modjeskas Due to Hepatitis A Risk

    Bauer's Candies, Inc. is recalling 1 lb salted combo modjeskas due to a risk of Hepatitis A exposure. The product was distributed to retail locations and private individuals in multiple states.

    Product
    1 lb salted combo modjeskas
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1195-2019·2019-04-03

    Bauer's Candies Recalls Sea Salt Modjeskas Due to Hepatitis A Risk

    Bauer's Candies, Inc. is recalling Sea Salt Modjeskas due to a risk of Hepatitis A exposure. The candy was distributed to retail locations and private individuals in multiple states.

    Product
    Sea Salt Bauer's Candies Modjeskas NET WT 8 oz bag, bulk, 4 oz bag, 1 lb, 2 lb, 8 oz box
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1201-2019·2019-04-03

    Bauer's Candies Recalls Candy Combos Due to Hepatitis A Exposure Risk

    Bauer's Candies, Inc. is recalling various candy combos due to a risk of Hepatitis A exposure. The products were distributed to retail locations and private individuals in multiple states.

    Product
    1 lb QVC combo, 1 lb combo, 2 lb combo, 12 oz combo, 8 oz combo, holiday combo
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1199-2019·2019-04-03

    Bauer's Candies Recalls Bulk Chocolate Caramels Due to Hepatitis A Risk

    Bauer's Candies, Inc. is recalling bulk chocolate caramels due to a risk of Hepatitis A exposure. The product was distributed to retail locations and private individuals in multiple states.

    Product
    bulk chocolate caramels
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1194-2019·2019-04-03

    Bauer's Chocolate Modjeskas Recalled for Hepatitis A Exposure Risk

    Bauer's Candies is recalling Chocolate Modjeskas due to a risk of Hepatitis A exposure. The products were distributed to retail locations and private individuals in multiple states.

    Product
    Bauer's Candies Chocolate Modjeskas NET WT 4 oz & 8 oz bags, 8 oz box, bulk, & 1 lb box
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-1198-2019·2019-04-03

    Bauer's Candies Recalls Bulk Assorted Candy Due to Hepatitis A Risk

    Bauer's Candies, Inc. is recalling 2 cases of bulk assorted candy due to a risk of Hepatitis A exposure. The product was distributed to retail locations and private individuals in multiple states.

    Product
    Bulk assorted
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Devices)·Z-1053-2019·2019-04-03

    Philips UroDiagnost MRF Recall Due to Missing Locking Plate

    Philips is recalling UroDiagnost MRF units because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.

    Product
    Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine examinations including: Urograms with injection or infusion Retrograde pyelography Cystography and urethrography Micturition…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1197-2019·2019-04-03

    Bauer's Candies Caramels Recalled for Hepatitis A Exposure Risk

    Bauer's Candies, Inc. is recalling specific caramel products due to a risk of Hepatitis A exposure. The affected items were distributed to retail locations and private individuals in multiple states.

    Product
    Bauer's Candies Caramels NET WT 4 oz (bag) & bulk, QVC 4 pack caramels
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-1193-2019·2019-04-03

    Bauer's Candies Recalled for Potential Hepatitis A Exposure Risk

    Bauer's Candies is recalling Modjeskas candies due to a risk of Hepatitis A exposure. The products were distributed to retail locations and private individuals in multiple states.

    Product
    Modjeskas Bauer's Candies NET WT 8 oz, 12 oz, 16 oz, 32 oz. boxes & 4 oz, 8 oz bags, 400 pc case, 216 pc case
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-1054-2019·2019-04-03

    Philips OmniDiagnost X-ray System Recalled for Missing Locking Plate

    Philips North America is recalling 1,696 OmniDiagnost Classic X-ray systems because a missing locking plate may cause unexpected stand or table movement that users cannot stop.

    Product
    Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system with remote-controlled facilities. It performs a wide range of routine examinations and interventional procedures include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1187-2019·2019-04-03

    Jacques Big Daddy Dark Chocolate Bar Recalled for Undeclared Milk

    Jacques Torres Manufacturing is recalling Big Daddy Dark Chocolate Bars because they contain undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped with reddish brown paper label.
    Category
    Food
    Distribution
    17 states
  • HighNHTSA·19V269000·2019-04-03

    Weis Fire & Safety Recalls One 2018 Ford F-550 Emergency Vehicle

    Weis Fire & Safety is recalling one 2018 Ford F-550 emergency vehicle because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    FORD — FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1071-2019·2019-04-03

    ICU Medical Recalls Transpac IV Monitoring Kits Due to Tubing Separation

    ICU Medical is recalling 280 Transpac IV Monitoring Kits because pressure tubing may separate, potentially causing blood loss or air embolism.

    Product
    ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60" Tubing, Disposable Transducer, 3 ml Squeeze Flush, Macrodrip (Pole Mount), REF: 42640-06, Sterile EO
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-1196-2019·2019-04-03

    Bauer's Candies Caramels Recalled for Hepatitis A Exposure Risk

    Bauer's Candies, Inc. is recalling Bourbon Sea Salt Caramels due to a risk of Hepatitis A exposure. The product was distributed to retail locations and private individuals in multiple states.

    Product
    Bourbon Sea Salt Bauer's Candies Caramels NET WT 4 oz & 8 oz (bag) & bulk
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-1066-2019·2019-04-03

    Beaver Visitec Soft Tip Cannula Recall for Missing Protective Sheath

    Beaver Visitec is recalling specific lots of Soft Tip Cannulas because a missing protective sheath may cause the silicone tip to break or detach during eye procedures.

    Product
    BVI Visitec Soft Tip Cannula, 0.8MM .50 x 33mm (25G x 1.3 in). The BVI Soft Tip Cannula is intended to irrigate and/or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate (e.g. retinal, subretinal procedures).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1068-2019·2019-04-03

    Medical Action Industries Recalls Laparotomy Sponges Due to Sterility Concerns

    Medical Action Industries is recalling specific lots of laparotomy sponges due to a potential lack of sterility assurance. The affected products were distributed nationwide and to Canada and Saudi Arabia.

    Product
    Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case) - Model Number 300, 450, SM40018, V300; 2. Lap 18X18 XR (5 each/pack, 40 pack/case) - Model Number 400, 404, V400, V450; 3. Lap 18X18 XR w/ring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1049-2019·2019-04-03

    LW Scientific ZIP IQ Combo Centrifuge Rotor Recall for Breakage Risk

    LW Scientific is recalling ZIP IQ Combo Centrifuges because the hematocrit rotor may break and eject through the housing, posing a safety hazard.

    Product
    LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-2RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes with additional rotor to spin other fluids in test tubes (15ml)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1051-2019·2019-04-03

    BD Synapsys Laboratory Software Recalled for Incorrect Test Order Association

    Becton Dickinson is recalling BD Synapsys version 2.1 because it allowed test orders to be associated with incorrect culture records.

    Product
    BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution providing data management and workflow management functionality across clinical diagnostic activities. The software integrates operational and clinical data…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1210-2019·2019-04-03

    Pillsbury Flour Recalled Due to Potential Salmonella Contamination

    Hometown Food Company is recalling Pillsbury Unbleached All Purpose Flour due to potential Salmonella contamination. The product was distributed nationwide.

    Product
    Pillsbury Unbleached All Purpose Flour Enriched 5Lb paper bag retail. 8 bags per shrink wrapped bale wholesale. UPC "0 5150022241 6" - retail unit UPC "0 5150022241 3" - wholesale bale
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2019·2019-04-03

    Accelerate Pheno System Recalled for Incorrect Meropenem Susceptibility Results

    Accelerate Diagnostics is recalling 81 Accelerate Pheno systems because rare bacterial isolates may generate incorrect meropenem susceptibility results. A software update suppresses these specific results to mitigate risk.

    Product
    Accelerate Pheno system, with Accelerate Pheno System Software 1.2.1 - 1.3.1, PSW000012B Product Usage: The Accelerate Pheno system is intended to measure signal intensity of fluorescent probes bound to nucleic acid in target and non-target organisms and to take time-lapse…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1060-2019·2019-04-03

    GE Healthcare Recalls Integrated ECG Cables Due to Short Circuit Risk

    GE Healthcare is recalling 288 integrated ECG cables that can short circuit during defibrillation, potentially diverting 25% of the energy away from the patient.

    Product
    Integrated ECG cable with 3-lead leadwires labeled as the following: 1. ECG TRUNK CABLE, 3-LD W/ INTEGRATED GRABBER LEAD WIRE, AHA, 3.6 M/12 FT; 2. ECG TRUNK CABLE, 3-LD W/ INTEGRATED GRABBER LEAD WIRE, IEC, 3.6 M/12 FT Product Usage: The reusable ECG trunk cable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2019·2019-04-03

    Philips MX40 Wearable Monitor Batteries Recalled for Manufacturing Defect

    Philips North America is recalling 40 lithium-ion rechargeable batteries for the MX40 Wearable Monitor due to a manufacturing defect that may affect monitor operation.

    Product
    Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor REF: 989803176201 - Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring and recording of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1186-2019·2019-04-03

    Klaire Labs Reduced L-Glutathione Recalled for Containing Lithium Orotate

    ProThera, Inc. is recalling Klaire Labs Reduced L-Glutathione capsules because they are mis-packaged and contain Lithium Orotate instead of the labeled ingredient.

    Product
    Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9
    Category
    Drug
    Distribution
    14 states