The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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11276–11300 of 13717

  • HighFDA (Devices)·Z-1557-2022·2022-08-24

    Echelon-14 Micro Catheter Recall Due to Moisture Exposure During Transport

    Micro Therapeutics is recalling Echelon-14 Micro Catheters because outer packaging was exposed to moisture during transport. The moisture exposure could compromise the sterility or function of the device.

    Product
    Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1541-2022·2022-08-24

    Skin liquid bandage recalled for improper temperature storage

    Family Dollar's NEW SKIN Liquid Bandage was not stored in temperature-controlled conditions, potentially compromising product integrity. Affected units were sold nationwide during May through June 2022.

    Product
    NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ, SKU 999417
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1523-2022·2022-08-24

    Power Electronic Box Subassembly Loose Screws Pose Electrical Shock Risk

    Myolyn Inc. is recalling the power electronic box subassembly for the MyoCycle MC-2 because internal mounting screws may come loose during shipping, creating a risk of electrical shock.

    Product
    Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-1556-2022·2022-08-24

    FDA Recalls Echelon-14 Microcatheters Due to Moisture-Exposed Packaging

    Micro Therapeutics is recalling Echelon-14 microcatheters whose outer carton packaging was exposed to a wet substance during transport, posing a risk to device sterility.

    Product
    Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1532-2022·2022-08-24

    CURAD First Aid Kit Recalls Due to Improper Storage Temperature

    Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.

    Product
    CURAD FIRST AID KIT, SKU 999037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1548-2022·2022-08-24

    Medical dressing tray mislabeled as latex-free but contains natural rubber latex

    Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.

    Product
    Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1528-2022·2022-08-24

    Veriquick Pregnancy Test 2CT Recalled for Improper Storage

    Family Dollar is recalling Veriquick Pregnancy Test 2CT kits (SKU 903756) sold from May 1 to June 10, 2022 due to improper storage outside temperature-controlled areas.

    Product
    Veriquick Pregnancy Test 2CT, SKU 903756
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2022·2022-08-24

    Abbott Alinity m Diagnostic System Recalled for Incorrect Optical Calibration

    Abbott Molecular is recalling the Alinity m System due to incorrect optical calibration. The affected unit (Serial Number 00654) was distributed to Italy.

    Product
    The Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1524-2022·2022-08-24

    ARIES SARS-CoV-2 Assay may produce false negative diagnostic results

    Luminex Corporation recalled 257 units of the ARIES SARS-CoV-2 Assay (lot AB4042A) due to potential false negative results. The assay may fail to detect the ORF1ab gene, risking missed COVID-19 infections.

    Product
    ARIES SARS-CoV-2 Assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2022·2022-08-24

    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT Recalled Due to Improper Temperature Storage

    Family Dollar is recalling LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT that were stored without proper temperature control. Customers should discontinue use of product purchased between May 1 and June 10, 2022.

    Product
    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT, SKU 900265
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1545-2022·2022-08-24

    Simply Saline Nasal Mist Recalled for Improper Storage Conditions

    Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.

    Product
    SIMPLY SALINE NASAL MIST 3.1 OZ, SKU 999801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1543-2022·2022-08-24

    GS Saline Solution recalled due to improper temperature storage

    GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.

    Product
    GS SALINE SOLUTION 12FL OZ, SKU 902274
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1540-2022·2022-08-24

    Contact Lens Solution Recalled for Improper Temperature Storage

    OPTI FREE REPLENISH contact lens solution sold at Family Dollar stores (May 1–June 10, 2022) was not stored in temperature-controlled areas and is being recalled.

    Product
    OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1533-2022·2022-08-24

    Clear Eyes Contact Lens Drops Recalled for Improper Storage

    Family Dollar Stores is recalling Clear Eyes Contact Lens Drops Lubricating due to improper storage in non-temperature-controlled areas. The product was sold nationwide between May 1 and June 10, 2022.

    Product
    CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO, SKU 900531
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1558-2022·2022-08-24

    Sensis Signal Input Box recall for patient electrical leakage hazard with improper mounting

    Siemens recalls 399 units of AXIOM Sensis systems due to risk of patient electrical shock if the Signal Input Box mounting deviates from its default position.

    Product
    AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo LOW 6634633; AXIOM Sensis, Combo 32 6634641; AXIOM Sensis, EP 129 6634658; Sensis 10764561
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1537-2022·2022-08-24

    First Response 2-Count Pregnancy Test Recalled for Improper Storage

    Family Dollar Stores is recalling First Response 2 CT pregnancy tests due to improper storage outside temperature-controlled areas. Affected products were sold nationwide between May 1 and June 10, 2022.

    Product
    FIRST RESPONSE 2 CT, SKU 902343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1527-2022·2022-08-24

    VeriQuick Pregnancy Tests Recalled Due to Improper Storage

    Family Dollar is recalling VeriQuick pregnancy tests that were not stored in temperature-controlled areas between April-June 2022. Improper storage conditions may affect test accuracy.

    Product
    VERIQUICK PREGNANCY TEST 1CT, SKU 901260, 939504
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1536-2022·2022-08-24

    CURAD Waterproof Bandages Recalled for Improper Storage

    Family Dollar is recalling CURAD waterproof bandages due to improper storage outside temperature-controlled conditions. The recall affects approximately 419 units sold nationwide between May 1 and June 10, 2022.

    Product
    CURAD STRNG WATRPRF STRIP 1IN 20CT, SKU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1534-2022·2022-08-24

    Denture Cleanser Tablets Recalled for Improper Storage Conditions

    Family Dollar is recalling GS Denture Cleanser tablets (green and overnight formulas) due to improper storage in non-temperature-controlled areas. Products sold May 1 - June 10, 2022 may be affected.

    Product
    GS DENTURE CLEANSER GRN TAB 40CT, SKU 906312 GS DENTURE CLEAN OVRNT TAB 40CT, SKU 906023
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1529-2022·2022-08-24

    Temporary Dental Filling Product Recalled for Improper Storage

    Family Dollar is recalling DENTEMP temporary dental filling products (SKU 902139) that were stored outside temperature-controlled conditions. The product was sold at Family Dollar stores nationwide between May and June 2022.

    Product
    DENTEMP ONE STEP .077OZ, SKU 902139
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1544-2022·2022-08-24

    Polident Denture Cleansers Recalled Due to Improper Storage

    Polident denture cleansers sold at Family Dollar stores nationwide are being recalled due to improper storage conditions. No illnesses or injuries have been reported.

    Product
    POLIDENT DENTURE CLEANSERS 84 CT, SKU 901634 POLIDENT DENTURE CLNS TAB 28CT, SKU 906131
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1547-2022·2022-08-24

    KY Jelly Lubricant Recalled for Improper Storage Conditions

    KY Jelly Lubricant 2 FL OZ (SKU 901443) distributed at Family Dollar stores was not stored in temperature-controlled areas. Consumers should discontinue use of product purchased between May–June 2022.

    Product
    KY JELLY LUBRICANT 2 FL OZ, SKU 901443
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1542-2022·2022-08-24

    At-home marijuana test strips recalled for improper storage

    Family Dollar is recalling at-home marijuana test strips (SKU 900752) that were stored outside temperature-controlled areas. Improper storage may affect test accuracy.

    Product
    AT HOME MARIJUANA TEST STRIP, SKU 900752
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1539-2022·2022-08-24

    Poligrip Denture Adhesive Products Recalled for Improper Storage Conditions

    Family Dollar Stores recalls multiple Poligrip denture adhesive products due to improper storage outside temperature-controlled areas. Affected products were sold between May 1 and June 10, 2022.

    Product
    POLIGRIP ADH CREAM FREE 2.4OZ, SKU 900334 POLIGRIP DENTURE ADHESIVE ORIGINAL 2.4OZ, SKU 900723 SUPER POLIGRIP ADH CREAM .75OZ, SKU 900085
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1399-2022·2022-08-17

    FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance

    The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.

    Product
    HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
    Category
    Medical Device
    Distribution
    Distributed nationwide