The Recall Desk

State

New York product recalls

73,737 recalls have nationwide distribution and so reach New York. 12,955 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,955
Critical
1,508
Severe
3,701
Most recent
2026-10-28

Of the 12,955 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 3,701 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,955 recalls whose distribution notice names New York specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32076–32100 of 86692

  • SevereFDA (Food)·F-1544-2020·2020-09-30

    Gilster-Mary Lee Recalls Organic Microwave Popcorn Due to Glass Contamination

    Gilster-Mary Lee Corp. is recalling specific brands of organic microwave popcorn because tempered glass pieces were found in the product.

    Product
    Microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Salted, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40611 2) Sprouts Farmers Market, Organic Salted Microwave…
    Category
    Food
    Distribution
    21 states
  • SevereFDA (Drugs)·D-1593-2020·2020-09-30

    Zanilast+ Gel Antiseptic Hand Sanitizer Recalled for Potential 1-Propanol Contamination

    Nanomateriales S.A. de C.V. is recalling 1,000 kg of Zanilast+ Gel Antiseptic Hand Sanitizer due to GMP deviations that may result in the presence of 1-propanol.

    Product
    Zanilast+ Gel Antiseptic Hand Sanitizer (70% Ethyl Alcohol) Packaged in 25 kg bottles, Distributed by Fujimura Trading S.A. DE C.V. Juventino Rosas 1902, Col. Caracol, 64810, Monterrey, N.L., Mexico Nanomateriales S.A. DE C.V. NDC 69912-006-01
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-3005-2020·2020-09-30

    Siemens Syngo.via RT Image Suite Software Recall for Calibration Offset Error

    Siemens is recalling Syngo.via RT Image Suite software due to a calibration offset error that could result in incorrect radiation dose or dose applied to the wrong location.

    Product
    Software: Syngo.via RT Image Suite software version VA30_SP02 with license T_RT_IMAGE_SUITE_PAT_MARK Intended Use: used as an advanced application on a SOM10 scanner SMN: 10496180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·20193·2020-09-30

    STIHL Recalls Mini-Cultivator Attachments Due to Laceration Hazard

    STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.

    Product
    STIHL BF-KM Mini-Cultivator attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V598000·2020-09-30

    BMW 2020-2021 Rearview Camera Software Obscures Rear View Image

    BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.

    Product
    BMW — BMW 530I, X3, X4, M550I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2985-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1346, Sterile EO, Rx Only, CE, UDI: 8022057015228 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3000-2020·2020-09-30

    ArthroCare Recalls SmartStitch Connectors Due to Manufacturing Error

    ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.

    Product
    Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2984-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1345, Sterile EO, Rx Only, CE, UDI: 8022057015204 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V601000·2020-09-30

    BMW recalls vehicles due to debris in hybrid battery cells

    BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.

    Product
    BMW — BMW, MINI 745LE, X5, 530E, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1542-2020·2020-09-30

    Gilster-Mary Lee Recalls Light Microwave Popcorn Due to Foreign Matter

    Gilster-Mary Lee Corp. is recalling specific lots of Full Circle and Nature's Promise light microwave popcorn because tempered glass pieces were found in the product.

    Product
    Light microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Light Butter, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40610 2) Nature's Promise, Microwave Popcorn…
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-3012-2020·2020-09-30

    Irvine Biomedical Recalls Steerable Diagnostic Catheters Due to Labeling Error

    Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.

    Product
    Inquiry Steerable Diagnostic Catheter, REF: IBI-87002 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2986-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 8022057015211 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20194·2020-09-30

    Petzl Recalls Low-Stretch Kernmantle Ropes Due to Fall and Injury Hazard

    Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.

    Product
    Low-Stretch Kernmantle Ropes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1541-2020·2020-09-30

    Gilster-Mary Lee Recalls Microwave Popcorn Due to Glass Contamination

    Gilster-Mary Lee Corp. is recalling Cadia and Lidl microwave popcorn because tempered glass fragments were found in the product.

    Product
    Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9 oz (281 g) 3-3.3 oz (94 g) bags, KeHDistributors LLC, Naperville, IL, UPC 15369-01288 2) Lidl, Naturally Flavored Butter Microwave Popcorn, 3-3.3 oz (94g)…
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-2990-2020·2020-09-30

    Hologic Recalls Panther Fusion Tube Trays Due to Potential Leaks

    Hologic is recalling 607 Panther Fusion Tube Trays because they may leak, potentially invalidating patient results or causing false negatives in flu and RSV assays.

    Product
    Panther Fusion Tube Tray, Part: FAB-15004, REF: PRD-04000
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Food)·F-1543-2020·2020-09-30

    Gilster-Mary Lee Recalls Buttered Microwave Popcorn Due to Glass Fragments

    Gilster-Mary Lee Corp. is recalling specific brands of buttered microwave popcorn because tempered glass fragments were found in the product.

    Product
    Buttered microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Butter, 3-3.3 oz (94 g) bags, Net Wt. 9.9 oz (281 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40609 2) Sprouts Farmers Market, Organic Butter…
    Category
    Food
    Distribution
    21 states
  • HighNHTSA·20V600000·2020-09-30

    2021 Entegra motorhomes recalled for power seat wiring fire risk

    Jayco is recalling 2021 Entegra motorhomes with Villa power seats because the electrical wiring may become damaged or chafed, causing short circuits and fire risk.

    Product
    ENTEGRA — ENTEGRA REATTA XL, ASPIRE, CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2988-2020·2020-09-30

    LivaNova Recalls Perceval Dual Collapser Due to Valve Collapse Failure

    LivaNova is recalling specific lots of the Perceval Dual Collapser because complaints indicate the device may fail to collapse the heart valve during implantation.

    Product
    Perceval Dual Collapser, Size S/M, REF: ICV1235, Sterile EO, Rx Only, CE, UDI: 08022057014832 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant, allowing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2987-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1350, Sterile EO, Rx Only, CE, UDI: 8022057015259 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2995-2020·2020-09-30

    GE Healthcare Recalls NM 830 Medical Detectors Due to Loose Screws

    GE Healthcare is recalling 25 NM 830 detectors because rotor bearing screws were found loose. The devices are distributed in the US and internationally.

    Product
    NM 830 Model # H3910AC
    Category
    Medical Device
    Distribution
    27 states