The Recall Desk

State

New York product recalls

73,366 recalls have nationwide distribution and so reach New York. 12,941 additional recalls listed New York specifically in their distribution scope.

What the numbers show

Total
12,941
Critical
1,511
Severe
3,698
Most recent
2026-10-07

Of the 12,941 recalls naming New York we have scored against our rubric, 1,511 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,698 (29%) are Severe.

Which agencies issued them

These figures cover only the 12,941 recalls whose distribution notice names New York specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18576–18600 of 86307

  • HighFDA (Devices)·Z-1497-2023·2023-05-10

    CryoTreQ Aa ophthalmic instrument recalled for risk of sudden disassembly

    Beaver Visitec is recalling the CryoTreQ Aa ophthalmic surgical instrument due to risk of sudden disassembly during use. Device disassembly during cryosurgery could cause permanent vision impairment.

    Product
    CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery. It creates a tip at cryogenic temperatures by evaporation of N2O that can be utilized to perform cryotherapy based on the destruction of tissue by extreme cold to locally perform cryocoagulation on…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0560-2023·2023-05-10

    Drug recall: Simvastatin 20 mg due to manufacturing control deviations

    PD-Rx Pharmaceuticals is voluntarily recalling 520 bottles of Simvastatin USP 20 mg nationwide due to manufacturing process quality control deviations. No adverse events have been reported.

    Product
    Simvastatin USP 20 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottles (NDC 43063-008-30), b) 90 count-bottles (NDC: 43063-0008-90)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2023·2023-05-10

    LINK SLED Knee Implant Component Recalled Due to Loosening

    Linkbio Corp. recalls the LINK SLED Knee Component due to risk of early aseptic loosening and implant wear. The issue stems from suboptimal implant positioning or inadequate cementing technique.

    Product
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X 50MM Item Number: 15-2028/07
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1477-2023·2023-05-10

    Philips ProxiDiagnost N90 radiography systems recalled due to cable damage

    Philips is recalling certain ProxiDiagnost N90 radiography systems due to a cable under the table that may break. A broken cable could prevent users from tilting the table or engaging braking.

    Product
    Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluoroscopy (R/F) system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0789-2023·2023-05-10

    Cargill Soy Flour Recalled for Undeclared Gluten Above Safe Levels

    Cargill is recalling PROSANTE soyflour products labeled gluten-free because they may contain gluten levels above 20 ppm, the FDA's threshold for gluten-free claims. People with celiac disease or gluten sensitivity should not consume these products.

    Product
    PROSANTE TSOYFLR 5P MNCD 50LB BG/21P, PROSANTE TSOYFLR 5P MNCD 25LB BG, PROSANTE TSOYFLR 5P MNCD 50LB BG, PROSANTE TSOYFLR 5P MNCD 800LB TT; distributed paper bags and bulk totes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2023·2023-05-10

    Walgreens assorted bandages recalled for undisclosed ingredient in adhesive

    ASO LLC is recalling Walgreens assorted bandages (item 196568) distributed nationwide due to benzalkonium chloride in the adhesive pad that is not disclosed on the labeling.

    Product
    WALGREENS BANDAGES, item number 196568, 110 CT VALUE PACK, 24 BOXES/MASTER (shipping container), Walgreens Family Pack ASSORTED BANDAGES, 110 ASSORTED SIZES (retail package)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0799-2023·2023-05-10

    Cargill recalls bulk ingredient for gluten exceeding safe levels

    Cargill recalls 174,600 lbs of bulk ingredient distributed nationwide and internationally. Products labeled gluten-free contain gluten levels exceeding 20 ppm.

    Product
    PROSANTE TVGPTN 7B MNCD 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2023·2023-05-10

    Steris surgical light handle covers may detach during procedures

    Steris surgical light handle covers may detach during use, risking contamination of the sterile field and patient injury. The FDA is recalling approximately 1.4 million affected covers.

    Product
    Steris Lighting and Visualization Systems, Sterile Light Handle Cover (LB53)- Surgical light handle covers, including disposable surgical light handle covers are designed to fit over surgical light handles for sterile surgeon control. REF: LB53
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0792-2023·2023-05-10

    Cargill PROSANTE vegetable protein recalled for undeclared gluten levels

    Cargill is recalling PROSANTE vegetable protein products labeled gluten-free due to potential gluten contamination exceeding 20 ppm. Consumers should check product codes and discard or return affected items.

    Product
    PROSANTE TVGPTN 12BF7 MNCD 50LB BG/36P, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1562-2023·2023-05-10

    Laboratory Automation Module Firmware May Cause Sample Misidentification

    Vesmatic Cube 80 laboratory automation system firmware can incorrectly identify patient samples, potentially leading to wrong test results and inappropriate treatment. Affected systems include FlexLab, Accelerator a3600, and Aptio Automation units.

    Product
    Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: 72747000.A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1508-2023·2023-05-10

    Linkbio LINK SLED Knee implant system recalled for surgical technique requirements

    Linkbio Corp. recalls LINK SLED Knee System implants due to risk of early loosening and increased wear caused by improper surgical technique. Updated training and labeling have been issued.

    Product
    LINK SLED Knee System: ENDO SLED KNEE FEM COMP, MEDIUM SMALL Item Number: 15-2020/46
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1523-2023·2023-05-10

    LINK SLED Knee System tibial component recall due to implant positioning and cementing concerns

    Linkbio Corp. is recalling LINK SLED Knee System tibial components due to risk of early loosening or increased wear caused by suboptimal implant positioning or inadequate cementing technique. Surgeons are being directed to update their technique and receive additional training.

    Product
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0798-2023·2023-05-10

    Cargill Soy Flour Recalled for Possible Gluten Contamination

    Cargill is recalling PROSANTE soy flour products labeled gluten-free because they may contain gluten levels above 20 ppm, the FDA's regulatory threshold for gluten-free labeling. Products were distributed nationwide and internationally.

    Product
    PROSANTE TSOYFLR 7P MNCD 25LB BG/40P, PROSANTE TSOYFLR 7P MNCD 50LB BG, 25 lb and 50lb paper bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2023·2023-05-10

    LINK SLED Knee Implant Component Recalled Due to Early Loosening Risk

    FDA recalls LINK SLED Knee System tibial components due to risk of aseptic loosening and premature wear. Patients may require revision surgery.

    Product
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 50MM Item Number: 15-2028/08
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0786-2023·2023-05-10

    Prosante TVGPTN Food Products Recalled for Potential Gluten Contamination

    Cargill is recalling Prosante TVGPTN food products labeled as gluten-free that may contain gluten above 20 ppm.

    Product
    PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF MNCD 50LB BG/36P, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0784-2023·2023-05-10

    Gluten-Free Labeled Poultry Ingredient May Contain Undisclosed Gluten

    Cargill is recalling PROSANTE TVGPTN 3018B FLK poultry ingredient because products labeled gluten-free may contain gluten levels above 20 ppm, the legal threshold for gluten-free claims.

    Product
    PROSANTE TVGPTN 3018B FLK 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2023·2023-05-10

    Knee implant system recall due to aseptic loosening from improper surgical technique

    Linkbio Corp. recalls LINK SLED Knee System tibial component due to risk of early aseptic loosening caused by inadequate surgical technique. Training on improved surgical technique is being provided.

    Product
    LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 50 MM Item Number: 15-2230/06
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0559-2023·2023-05-10

    Drug Recall: Glimepiride 4 mg for Manufacturing Practice Deviations

    PD-Rx Pharmaceuticals is recalling 186 bottles of Glimepiride USP 4 mg due to manufacturing deviations. Patients using this medication should contact their healthcare provider to verify if their supply is affected.

    Product
    Glimepiride USP, 4 mg, 90 count-bottles, Rx only, Intas Pharm. Limited Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0587-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0557-2023·2023-05-10

    Drug Recall: Montelukast Sodium Tablets Due to Manufacturing Deviations

    PD-Rx Pharmaceuticals has recalled 352 bottles of Montelukast Sodium USP 10 mg tablets distributed nationwide due to manufacturing process deviations. This was a voluntary recall by the firm.

    Product
    Montelukast Sodium USP, 10 mg, 30 count-bottles, Rx only, Intas Pharm, Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0762-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0563-2023·2023-05-10

    Advil Ibuprofen Tablets Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling Advil Ibuprofen 200 mg tablets due to a storage temperature deviation during manufacturing and distribution. No illnesses have been reported.

    Product
    Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1556-2023·2023-05-10

    VITROS 5600 system pack opener assembly may not function properly

    The MicroTip Pack Opener Assembly on VITROS 5600 systems may fail to remove or replace pack caps properly, making packs unusable and delaying clinical test results. Approximately 4,895 units were distributed.

    Product
    VITROS 5600 Integrated System- For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents and VITROS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1557-2023·2023-05-10

    VITROS 5600 Integrated System MicroTip Pack Opener Assembly Defect

    Refurbished VITROS 5600 diagnostic systems may have a defective MicroTip Pack Opener Assembly that fails to properly remove or replace pack caps, potentially causing delayed test results. Ortho-Clinical Diagnostics is recalling 1,148 units distributed nationwide and internationally.

    Product
    VITROS 5600 Integrated System - Refurbished . For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0808-2023·2023-05-10

    Atkins Milk Chocolate Delight Protein Shakes Recalled for Spoilage Risk

    Simply Good Foods is recalling Atkins Milk Chocolate Delight Protein Shakes nationwide due to post-processing contamination that may cause spoilage. Affected products have lot numbers SA2208P3F6 (exp. 07/27/23) or SA2210P3F6 (exp. 07/29/23).

    Product
    Atkins Milk Chocolate Delight Protein Rich Shakes, NET WT. 44 oz (4 / 11oz), 4 Tetra Packs per carton, UPC 637480065016, Distributed exclusively by Simply Good Foods USA, Inc. Denver, CO 80202, 1-800-6-ATKINS
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0565-2023·2023-05-10

    Advil Dual Action Pain Reliever Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling Advil Dual Action pain reliever tablets (36-caplet bottles, SKU 0902867) nationwide because the product was stored outside labeled temperature requirements.

    Product
    Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles
    Category
    Drug
    Distribution
    Distributed nationwide