The Recall Desk

State

New York product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37151–37175 of 86696

  • HighFDA (Devices)·Z-0124-2020·2019-10-23

    Integra LifeSciences Recalls Cerelink ICP Monitor Due to Reading Decline

    Integra LifeSciences is recalling 189 Cerelink ICP Monitor units because they may show a progressive decline in intracranial pressure readings during use.

    Product
    Cerelink ICP Monitor, Model Number 826820; intended for use as an interface between compatible strain-gauge type pressure transducers and standard physiological pressure monitoring systems.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-0060-2020·2019-10-23

    G&C Food Distributors Recalls Frozen Blackberries Due to Norovirus Contamination

    G&C Food Distributors is recalling 299 cases of frozen blackberries because the product is contaminated with norovirus. The affected bags were distributed to retailers in nine states and Belize.

    Product
    Frozen blackberries, packaged in 16 ounce (454 gram) plastic bags (12 bags per master case). Plastic bags labeled with: PREMIUM QUALITY, KEEP FROZEN, NON-GMO, CORNERSTONE PREMIUM FOODS, Blackberries, GREAT FOR SMOOTHIES, NET WEIGHT 16 OZ. (454g), INGREDIENTS: BLACKBERRIES…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0128-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set Yellow Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, Secure Lock, 107 Inch. 1 unit per pouch; 48 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0134-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers 19,350 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 1.2 Micron Filter Set Non-Vented, Microbore, PAV, 123 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0136-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filters. The affected units were distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as PRIMARY PLUMSET 15 Micron Filter in Sight Chamber, CLAVE Port, 0.2 Micron Filter, CLAVE Y-Site, PE Lined Light Resistant Tubing, Distal Microbore Tubing 272 cm / 15 mL.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0131-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0130-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets with inline filters because fluid may leak out of the air vents. The recall covers 45,900 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Primary 0.2 Micron Filter Set, Microbore, CLAVE Y-Site, 118 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0052-2020·2019-10-23

    Jansal Valley Snack Mix Recalled for Incorrect Allergen Labeling

    Friendly Fruit Market is recalling Jansal Valley Energize Snack Mix because the label lists allergens that are not actually in the product.

    Product
    Jansal Valley brand Energize Snack Mix NET WT 5 OZ (142 G) in plastic clamshells, Ingredients: apricots, almonds, banana chips, coconut, cashews, dates, raisins, hazelnuts, pecans, pepitas, walnuts, papaya, pineapple. Contains: almonds, cashews, coconut, hazelnuts, pecans…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0138-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents. The recall covers 6,400 units distributed in the U.S. and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, CLAVE Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0139-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling 521 units of Plum Microbore Infusion Sets because air vents on inline filters may leak fluid. The recall covers nationwide and international distribution.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0127-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage

    ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filter air vents.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 0.2 Micron Filter, Prepierced Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock, 104 Inch. 1 unit per pouch; 50…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0146-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling Sapphire Microbore Infusion Sets with Inline Filters due to a potential for fluid leakage out of air vents.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case. Not distributed in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0036-2020·2019-10-23

    Gullah Gourmet Recalls Nana's Been a Nut Bread for Missing Walnut Labeling

    Gullah Gourmet, Inc. is recalling 673 bags of Nana's Been a Nut Bread because the ingredient statement does not list walnuts, posing a risk to consumers with walnut allergies.

    Product
    Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS CONTAINING WHEAT, EGGS, MILK, SOY AND TREE NUTS. GULLAH BOURMET Inc. CHARLESTON, SC 29407 UPC 6 50305 01045 9
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0051-2020·2019-10-23

    Jansal Valley Snack Mix Recalled for Incorrect Allergen Labeling

    Friendly Fruit Market is recalling Jansal Valley Indulgent Snack Mix because the label lists allergens not actually in the product.

    Product
    Jansal Valley brand Indulgent Snack Mix NET WT 12 OZ (340 G) in plastic clamshells, Ingredients: apricots, almonds, banana chips, coconut, cashews, dates, raisins, hazelnuts, pecans, pepitas, walnuts, papaya, pineapple. Contains: almonds, cashews, soy. This product is packaged…
    Category
    Food
    Distribution
    9 states
  • HighNHTSA·19V755000·2019-10-23

    BMW Recalls 2020 330i and M340i for Trunk Release Cable Defect

    BMW is recalling 2020 330i and M340i vehicles because an improperly installed trunk release cable may prevent the trunk from opening from the inside.

    Product
    BMW — BMW 330I, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0143-2020·2019-10-23

    ICU Medical Recalls Sapphire Microbore Infusion Sets Due to Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filter air vents. The product was distributed in the U.S. and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set Yellow-Striped Microbore, 0.2 Micron Filter 301 cm / 8.3 mL. 1 unit per blister; 40 blisters per case . Not distributed in the U.S.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0125-2020·2019-10-23

    OrthoPediatrics Recalls Adolescent Attachment Bolts Due to Interference Risk

    OrthoPediatrics Corp is recalling 211 units of Adolescent attachment bolts used with the Pediatric Nailing Platform. The recall is due to potential interference between the bolt and nail, which may delay surgical procedures.

    Product
    OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing Platform (PNP) targeting arm- intended as an orthopedic implant system (bolt is used to attach the targeting arm to the intramedullary fixation rod) Part number: 01-1503-0032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter, PAV, 123 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0135-2020·2019-10-23

    ICU Medical Recalls Sapphire Infusion Sets Due to Fluid Leakage Risk

    ICU Medical is recalling Sapphire Microbore Infusion Sets because fluid may leak from the inline filters. The recall covers 4,600 units distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Sapphire Microbore Infusion Sets with Inline Filters labeled as SAPPHIRE Epidural Set with NRFit Connector Yellow-Striped Microbore, 0.2 Micron Filter 119 Inch. 1 unit per pouch; 50 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0137-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Fluid Leakage Risk

    ICU Medical Inc is recalling specific Plum Microbore Infusion Sets because fluid may leak from the inline filters. The affected units were distributed nationwide and internationally.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, CLAVE Y-Site, Polyethylene Lined Light Resistant Tubing, Distal Microbore…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0145-2020·2019-10-23

    ICU Medical Recalls Plum Microbore Infusion Sets Due to Leakage Risk

    ICU Medical Inc is recalling 7,920 units of Plum Microbore Infusion Sets because fluid may leak from the inline filters.

    Product
    Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as PLUM Epidural Set with NRFit Connector Yellow-Striped Tubing, Distal Microbore Tubing, 0.2 Micron Filter, 107 Inch. 1 unit per pouch; 48 pouches per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0148-2020·2019-10-23

    Siemens Atellica CH 930 Analyzer Recalled for Erroneous Hemolysis and Lipemia Indices

    Siemens Healthcare Diagnostics is recalling 1,125 Atellica CH 930 Analyzers worldwide due to software errors that may produce incorrect hemolysis and lipemia indices.

    Product
    Siemens Atellica CH 930 Analyzer. Siemens Material Number (SMN): 11067000 Product Usage: automated, clinical chemistry analyzer to perform in vitro diagnostic tests on clinical specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0151-2020·2019-10-23

    Xodus Medical Recalls Cautery Tip Cleaners Due to Sterile Barrier Concerns

    Xodus Medical Inc is recalling 255,000 Cautery Tip Cleaners because the sterile barrier of some devices may have been affected.

    Product
    Cautery Tip Cleaner REF: 30500 Product Usage: electrosurgical accessory
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0150-2020·2019-10-23

    Xodus Medical Recalls Electrosurgical Tip Cleaners Due to Sterile Barrier Concerns

    Xodus Medical Inc is recalling 460,000 Electrosurgical Tip Cleaners because the sterile barrier of some devices may have been affected.

    Product
    Electrosurgical Tip Cleaner REF: 62-8499-001 Product Usage: electrosurgical accessory
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0159-2020·2019-10-23

    Olympus Berkeley Disposa-Filter Recall Due to Weld Defect

    Olympus is recalling Berkeley Disposa-Filters used with the VC-10 Vacuum Curettage System because an ultrasonic weld defect may cause the housing to separate.

    Product
    Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System - Product Usage: designed for rapid transcervical aspiration of the uterine cavity. Part# 54298-10/pack
    Category
    Medical Device
    Distribution
    Distributed nationwide