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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9601–9625 of 113902

  • ModerateFDA (Drugs)·D-0388-2025·2025-04-30

    Duloxetine Delayed-Release Capsules Recalled for Nitrosamine Impurity

    Breckenridge Pharmaceutical is recalling Duloxetine Delayed-Release Capsules 30 mg nationwide due to the presence of a nitrosamine drug substance related impurity above proposed interim limits.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0726-2025·2025-04-30

    Texas Olive Co. Pepperoncini 16 oz Glass Jars Recalled

    All American Trading Of Houston, Inc. is recalling Texas Olive Co. Pepperoncini 16 oz glass jars due to potential contamination from non-heat-sealed sealing methods. The recall affects products sold in Texas and Mississippi.

    Product
    Texas Olive Co. Pepperoncini 16 oz glass jars
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0727-2025·2025-04-30

    Texas Olive Company Capers Capote recalled due to contamination risk

    Texas Olive Company Capers Capote in 8 oz. plastic containers and 16 oz. glass jars is being recalled because the repacking and sealing methods pose a possible risk of contamination.

    Product
    Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expiry prior to 06/04/2025 Texas Olive Company Capers Capote 16 oz. glass jar. All lots with expiry prior to 12/21/2025
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0386-2025·2025-04-30

    Bimatoprost Bulk Powder Recalled by Medisca for CGMP Deviations

    Medisca Inc. is voluntarily recalling Bimatoprost bulk powder in three sizes due to manufacturing process deviations. The powder was distributed nationwide.

    Product
    Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1646-2025·2025-04-30

    Zimmer Biomet Ceramic Femoral Head Hip Prosthesis Labeling Recall

    Zimmer, Inc. is recalling a ceramic femoral head hip prosthesis (Model 802602203) because product labeling lacks compatibility information for use with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0736-2025·2025-04-30

    Mexican Street Corn Soup recalled for possible wood contamination

    Request Foods Incorporated is recalling Mexican Street Corn Soup due to potential contamination with foreign material (wood). The product was distributed in Illinois and Michigan.

    Product
    Mexican Street Corn Soup, 4 / 4lb pouches, Net Wt. 16lb
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1640-2025·2025-04-30

    Merit Medical EsophyX Z+ Fastener Delivery Device Safety Update

    Merit Medical is updating instructions for the EsophyX Z+ Fastener Delivery Device due to risks associated with device over-rotation and multiple fastener deployment.

    Product
    Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0375-2025·2025-04-30

    Hemopropin Ointment Recalled Due to Manufacturing Process Deviations

    Apipharma is voluntarily recalling Hemopropin Ointment due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The recall affects specific lot numbers distributed in Arizona.

    Product
    Hemopropin Ointment, Lanolin 17.76% and Petrolatum 71.2%, Net Wt. 0.7 oz (20g) tubes, Manufactured by: Apipharma d.o.o, Croatia, Distributed by: Apipharma, LLC, Tempe, AZ UPC 3 858882 103534 and UPC 3 858882 101318
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1649-2025·2025-04-30

    Zimmer Biomet Ceramic Hip Head 22.2 mm Lacks Stem Compatibility Information

    Zimmer, Inc. is recalling a ceramic hip prosthesis head because the product labeling does not adequately describe compatibility with certain femoral stems used in hip replacement surgery.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1666-2025·2025-04-30

    Tempus Pro Patient Monitor software error when using video laryngoscope

    Remote Diagnostic Technologies Ltd. is recalling Tempus Pro Patient Monitors due to a software issue that causes an error screen when a video laryngoscope is attached to the device.

    Product
    Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)],
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0735-2025·2025-04-30

    Moroccan Style Lentil Soup recalled for potential wood contamination

    Request Foods Incorporated is recalling Moroccan Style Lentil Soup due to potential contamination with wood fragments. The product was distributed in Illinois and Michigan.

    Product
    Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0379-2025·2025-04-30

    DoloDent Maximum Strength Toothache Drops Recalled for cGMP Deviations

    Pharmadel, LLC is recalling DoloDent Maximum Strength Toothache Drops due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall affects 9,504 bottles distributed in Delaware.

    Product
    DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-400-15
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1647-2025·2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Heads Lack Stem Compatibility Information

    Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0377-2025·2025-04-30

    Clomipramine Hydrochloride Capsules recalled for degradation product specification failure

    Lupin Pharmaceuticals is recalling Clomipramine Hydrochloride Capsules (25 mg) due to an unspecified degradation product detected in stability testing. The defect was identified during an 18-month long-term stability study.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE CAPSULES)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1641-2025·2025-04-30

    Merit Medical EsophyX Z+ Fastener Delivery Device Instructions Update

    Merit Medical has updated instructions for the EsophyX Z+ fastener delivery device to provide additional information about risks associated with device over-rotation and multiple fastener deployment.

    Product
    Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO,RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0740-2025·2025-04-30

    Frozen Chopped Cilantro Recalled for Potential Foreign Object Contamination

    Supherb Farms is recalling frozen chopped cilantro due to potential contamination with foreign objects. Consumers should not use the product and should discard it or return it to the retailer.

    Product
    Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT: 2 lb; PERISHABLE - KEEP FROZEN; Packaging: 4 - 8 oz ziploc plastic bags in a white cardboard box; Net Wt. 2 lb
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Food)·F-0739-2025·2025-04-30

    IQF Cilantro Large Recalled Due to Foreign Object Contamination

    Supherb Farms is recalling frozen cilantro (IQF Cilantro Large, 30 lb packages) distributed across the United States, Canada, and Mexico due to potential contamination with foreign objects.

    Product
    Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard box
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1664-2025·2025-04-30

    Beckman Coulter DxI 9000 Access Immunoassay Analyzer communication loss

    Beckman Coulter DxI 9000 Access Immunoassay Analyzer may lose connection to laboratory information systems, interrupting sample processing and delaying patient test results.

    Product
    Beckman Coulter DxI 9000 Access Immunoassay Analyzer
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0382-2025·2025-04-30

    Rapidol Arnica Gel topical homeopathic medicine recalled for manufacturing violations

    Pharmadel, LLC is recalling Rapidol Arnica Gel (2 oz, 57 g) distributed in Delaware due to manufacturing process deviations. The voluntary recall affects 6,048 bottles of lot EAG-01 with expiration date MAR 27.

    Product
    Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0376-2025·2025-04-30

    Kapsin Ointment Drug Recalled Due to Manufacturing Process Deviations

    Apipharma is voluntarily recalling Kapsin Ointment (Camphor 3.16% and Capsaicin 0.03%) distributed in Arizona due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Kapsin Ointment, Camphor 3.16% and Capsaicin 0.03%. Net Wt. 2 oz (60g) tubes, Manufactured by: Apipharma d.o.o, Jeronima Kavanjina 26, 10090 Zagreb, Croatia, Distributed by: Apipharma, LLC, 2331 West Alameda Drive, Tempe, AZ 85282 UPC 3 858882 101363
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0380-2025·2025-04-30

    DoloEar Homeopathic Earache Drops Recalled for cGMP Deviations

    Pharmadel, LLC is recalling DoloEar Homeopathic Earache Drops (0.50 oz, 15 mL) due to cGMP (current Good Manufacturing Practice) deviations. The recall affects 27,648 bottles distributed in Delaware.

    Product
    DoloEar Earache Drops, Homeopathic, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-401-15
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0385-2025·2025-04-30

    HYDROmorphone Hydrochloride 50 mg Cassettes Recalled for Superpotency

    OurPharma LLC is recalling HYDROmorphone Hydrochloride 50 mg/50 mL cassettes nationwide because the assay results showed higher potency than specification.

    Product
    HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0383-2025·2025-04-30

    Rapidol Arnica Tablets recalled due to manufacturing deviations

    Pharmadel is recalling 6,048 bottles of Rapidol Arnica Tablets homeopathic medicine due to current good manufacturing practice (cGMP) deviations. The recall affects bottles with lot EAT-01, expiration date March 27, distributed in Delaware.

    Product
    Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1648-2025·2025-04-30

    Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Compatibility Labeling

    Zimmer, Inc. is recalling a ceramic femoral head for hip prosthesis (Model 802802202, 22.2 mm) because product labeling does not adequately describe compatibility with certain metal femoral stems.

    Product
    Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0378-2025·2025-04-30

    Clindamycin HCl 300 mg Capsule Recalled for CGMP Deviations

    RemedyRepack Inc. is recalling Clindamycin HCl 300 mg Capsules due to current Good Manufacturing Practice (CGMP) deviations. The recall affects approximately 1,858 30-count blister cards distributed in Pennsylvania.

    Product
    Clindamycin HCl, 300 mg Capsule, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC; 70518-3772-00
    Category
    Drug
    Distribution
    1 state