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.

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.

45026–45050 of 86773

  • ModerateUSDA FSIS·052-2018·2018-06-21

    Agri Star Recalls Beef Pastrami Due to Processing Deviation

    Agri Star Meat and Poultry is recalling approximately 3,592 pounds of ready-to-eat beef pastrami due to possible underprocessing and inadequate curing.

    Product
    Agri Star Meat and Poultry, LLC — Agri Star Meat And Poultry LLC Recalls Beef Pastrami Products due to Possible Processing Deviation
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0864-2018·2018-06-20

    Inopak Recalls Antibacterial Foaming Hand Wash Due to Microbial Contamination

    Inopak Ltd is recalling Option Systems Antibacterial Foaming Hand Wash because FDA analysis found out-of-specification microbial counts.

    Product
    Option Systems Antibacterial Foaming Hand Wash with .3% PCMX, 1000 mL pouches, Inopak, LTD, Ringwood, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2212-2018·2018-06-20

    Angiodynamics Recalls RS Tandem 5F DL Xcela PICC Catheters

    Angiodynamics Inc. is recalling 13 boxes of RS Tandem 5F DL Xcela PICC catheters because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS TANDEM 5F DL XCELA PICC PASV, Catalog Number 60M181582
    Category
    Medical Device
    Distribution
    34 states
  • SevereNHTSA·18E043000·2018-06-20

    TRW Air Bag Control Unit Recall for Hyundai and Kia Vehicles

    TRW is recalling air bag control units in certain Hyundai and Kia vehicles because electrical overstress may prevent air bags and seat belt pretensioners from deploying in a crash.

    Product
    AIR BAGS: AIR BAG/RESTRAINT CONTROL MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2217-2018·2018-06-20

    Angiodynamics Recalls PICC Nursing Trays Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 2 boxes of CAN 5F DL BIOFLO PASV PICC Nursing Trays because a component may contain unsafe levels of bacterial endotoxins.

    Product
    CAN 5F DL BIOFLO PASV PICC NURSING TRAY, Catalog Number 60M700936
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2210-2018·2018-06-20

    Angiodynamics Recalls 5F DL BIOFLO PICC Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 5F DL BIOFLO PICC kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    5F DL BIOFLO PICC, Catalog Number 60M180592
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2218-2018·2018-06-20

    Angiodynamics Recalls XCELA PICC Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 17 boxes of CAN 5F SINGLE XCELA PICC kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    CAN 5F SINGLE XCELA PICC, Catalog Number 60M701531
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2202-2018·2018-06-20

    Angiodynamics Recalls Bioflo Midline Catheters Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 3 boxes of RS - TANDEM 5F DL BIOFLO MIDLINE catheters because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2196-2018·2018-06-20

    Angiodynamics Recalls Bio-Stable Kits Due to Bacterial Endotoxin Risk

    Angiodynamics Inc. is recalling 298 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG, Catalog Number 45-895
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0861-2018·2018-06-20

    Acne Shave 3 Step Shaving System Recalled for Bacterial Contamination Risk

    Shadow Holdings DBA Bocchi Labs is recalling the Acne Shave 3 Step Shaving System due to CGMP deviations that may result in bacterial contamination.

    Product
    Acne Shave 3 Step Shaving System, contains one tube Acne Shave (salicylic acid) Shave Cream Acne Shield, one tube Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5% tube, and one Power Shaver per box, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0855-2018·2018-06-20

    Medline recalls flushable personal cleaning cloths due to microbial contamination

    Medline Industries is recalling specific lots of READYFLUSH PROTECT flushable personal cleaning cloths because of microbial contamination in a non-sterile product.

    Product
    READYFLUSH PROTECT with Dimethicone (3.2%), Flushable Personal Cleaning Cloths, 24-count flexible pack. Manufactured by Medline Industries, Inc. Mundelein, IL 60060 USA. NDC 53329-066-58.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0875-2018·2018-06-20

    Allergan Recalls Taytulla Contraceptive Softgels Due to Out-of-Sequence Tablets

    Allergan is recalling Taytulla softgel capsules because the tablets are out of sequence. This affects 168,768 blister cards distributed nationwide.

    Product
    TAYTULLA — TAYTULLA (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL, AND FERROUS FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2192-2018·2018-06-20

    Angiodynamics Recalls Bio-Stable Kits Due to Bacterial Endotoxin Risk

    Angiodynamics Inc. is recalling 17 boxes of Bio-Stable 5F kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2228-2018·2018-06-20

    Seaberg SAM XT-C Tourniquet Recalled for Potential Buckle Stitch Failure

    The Seaberg Company is recalling SAM XT-C tourniquets because internal testing showed stitches securing the buckle could fail, posing a risk of serious injury or death.

    Product
    Part #: SAM XT-C, Model: Hi-Viz Blue
    Category
    Medical Device
    Distribution
    23 states
  • SevereFDA (Devices)·Z-2223-2018·2018-06-20

    Angiodynamics Recalls BioFlo PICC Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling BioFlo PICC nursing kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (NV) 5FDL-55cm Maximal Barrier Nursing Kit w/70cm Nitinol Wire PG, Catalog Number 75-033
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0860-2018·2018-06-20

    Acne Shave Shave Cream Recalled for Potential Bacterial Contamination

    Shadow Holdings DBA Bocchi Labs is recalling Acne Shave Shave Cream due to CGMP deviations that may allow bacterial contamination.

    Product
    Acne Shave (salicylic acid) Shave Cream Acne Shield, 0.5%, 5.1 FL OZ (150 mL) tube, Distributed by: United Exchange Corp., 17311 Valley View Blvd, Cerritos, CA 90703 USA, UPC 7 80707 73111 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2213-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL XPP Kits Due to Bacterial Endotoxins

    Angiodynamics Inc. is recalling 5 boxes of RS 5F DL XPP Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL XPP KIT, Catalog Number 60M183104
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2214-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 104 boxes of RS 5F DL BIOFLO PASV kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M183481
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2205-2018·2018-06-20

    Angiodynamics Recalls RS 5F DL BIOFLO PASV Kits Due to Endotoxins

    Angiodynamics Inc. is recalling 2 boxes of RS 5F DL BIOFLO PASV kits because components may contain unsafe levels of bacterial endotoxins.

    Product
    RS 5F DL BIOFLO PASV, Catalog Number 60M132324
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2222-2018·2018-06-20

    BioFlo PICC Nursing Kit Recalled for Unsafe Bacterial Endotoxin Levels

    Angiodynamics Inc. is recalling BioFlo PICC Nursing Kits because a component may contain unsafe levels of bacterial endotoxins.

    Product
    BioFlo PICC (NV) 5FSL-55cm Maximal Barrier Nursing Kit w/ 70cm Nitinol Wire PG, Catalog Number 75-032
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0854-2018·2018-06-20

    PharMEDium Recalls Hydromorphone Syringes Due to Potency Issues

    PharMEDium Services is recalling 2,800 hydromorphone syringes nationwide because some units were found to be superpotent or subpotent.

    Product
    HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services, LLC, Dayton, NJ
    Category
    Drug
    Distribution
    Distributed nationwide