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.

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451–475 of 26077

  • SevereFDA (Food)·H-0813-2026·2026-05-27

    Fontana Flavors Parmesan Cheese Flavoring Recalled for Salmonella

    Fontana Flavors is recalling a parmesan cheese flavoring ingredient made with Salmonella-contaminated milk powder. The product was distributed in Illinois, Tennessee, and Canada for further processing.

    Product
    C7139D1 Natural Parmesan Cheese Flavor, Net Weight: 50 lbs. bags. Item #: 202405. For Further Processing. Fontana Foods, Janesville, WI.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0815-2026·2026-05-27

    PS Seasoning Smokehouse Unit recalled for Salmonella in milk powder

    PS Seasoning & Spices is recalling the Original Smokehouse Unit nationwide due to Salmonella contamination in a milk powder ingredient. No illnesses have been reported.

    Product
    1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2218-2026·2026-05-27

    Medtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk

    Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0820-2026·2026-05-27

    Solina Sourdough Cheese Crouton Seasoning Recalled Due to Salmonella Contamination

    Solina U.S. Holding is recalling 30 bags of Sourdough Cheese Crouton Seasoning due to potential Salmonella contamination. Lot 355048 with use-by date 7/8/2026 was distributed to MI, WI, PA, IL, GA, CA, and KS.

    Product
    Solina 6035415 Sourdough Cheese Crouton Seasoning, 50lb bag
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·H-0816-2026·2026-05-27

    PS Seasoning Jalapeno Heat Unit Recalled for Salmonella Contamination

    PS Seasoning & Spices is recalling its 1P Jalapeno Heat Unit seasoning nationwide because it was made with milk powder contaminated with Salmonella. Consumers should not use this product.

    Product
    1P Jalapeno Heat Unit for 300 lbs of Meat, Part #: 180002945. Net Wt 18 lbs (8.20kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0545-2026·2026-05-27

    Erythromycin 500 mg Tablets Recalled for Impurity Above Limits

    Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.

    Product
    ERYTHROMYCIN — ERYTHROMYCIN (ERYTHROMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0546-2026·2026-05-27

    CIMZIA injection recalled due to lack of sterility assurance

    UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.

    Product
    CIMZIA — CIMZIA (CERTOLIZUMAB PEGOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2202-2026·2026-05-27

    Swan-Ganz Catheters Models 131F7 Through AIQSGF8 Recalled Nationwide

    Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.

    Product
    Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0782-2026·2026-05-27

    Liquid Blenz Soursop Bitters Recalled Due to Botulism Risk

    Liquid Blenz Soursop Bitters 16 oz and 32 oz bottles may be under-processed, allowing Clostridium botulinum to grow. The product also lists unauthorized health claims. Consumers should not consume and should return bottles.

    Product
    Liquid Blenz Soursop Bitters 16 oz and 32 oz.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0808-2026·2026-05-27

    Liposomal Sleep Spray Recalled for Potential Bacterial Contamination and Botulism Risk

    Wellnov Supplements LLC is recalling Liposomal Sleep Spray due to manufacturing deviations that could allow bacterial pathogens and C. Botulinum contamination. No illnesses have been reported.

    Product
    Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0787-2026·2026-05-27

    Immunity Enhancer Elderberry Recall Due to Botulism Risk

    LIQUID BLENZ CORP is recalling Immunity Enhancer Elderberry in 16 oz and 32 oz sizes due to potential under-processing that may allow Clostridium botulinum growth. Approximately 18,190 bottles were distributed in New York and online.

    Product
    Immunity Enhancer Elderberry 16 oz and 32 oz.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2220-2026·2026-05-27

    Medtronic DLP Retrograde Cannula 13FR Model 94913L Recall

    Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0807-2026·2026-05-27

    Liposomal B12 Spray Recalled for Potential Bacterial and Botulinum Contamination

    Wellnov Supplements LLC is recalling Liposomal B12 Spray (30 ml, lot MB1024) distributed nationwide and in Puerto Rico due to manufacturing deviations that could lead to bacterial and C. Botulinum contamination. No illnesses have been reported.

    Product
    Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0794-2026·2026-05-27

    Liquid Blenz Good Brain Tonic Recalled Due to Botulism Risk

    Liquid Blenz Good Brain Tonic may contain Clostridium botulinum due to under-processing. Affected bottles were distributed in New York and sold online.

    Product
    Liquid Blenz Good Brain Tonic 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0795-2026·2026-05-27

    Joint Nourish Dietary Supplement Recalled for Botulism and Bacterial Contamination Risk

    Wellnov Supplements recalled Joint Nourish due to manufacturing deviations that could allow bacterial pathogen and botulinum contamination. Affected lot is JN0925, distributed nationwide.

    Product
    Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0793-2026·2026-05-27

    Flat Belly Bully Beverage Recalled for Botulism Risk

    Flat Belly Bully 16 oz and 32 oz bottles are recalled due to potential under-processing that could allow Clostridium botulinum growth. Approximately 18,190 bottles were distributed in New York and through online sales.

    Product
    Flat Belly Bully 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0801-2026·2026-05-27

    Liposomal Collagen Booster Recalled for Possible Bacterial Contamination

    Wellnov Supplements is recalling Liposomal Collagen Booster due to manufacturing defects that could allow bacterial contamination, including C. botulinum.

    Product
    Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2026·2026-05-27

    Oncology Kit With Extension Sets May Leak During Infusion Therapy

    ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.

    Product
    Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0790-2026·2026-05-27

    Prostate Bully Drink Recalled for Potential Clostridium botulinum Contamination

    LIQUID BLENZ CORP is recalling Prostate Bully in 16 oz and 32 oz bottles (18,190 units) due to potential Clostridium botulinum growth from under-processing. Products were distributed in New York and through online sales.

    Product
    Prostate Bully 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0791-2026·2026-05-27

    Pure Shilajit Tonic Recalled for Potential Botulism Risk and Health Claims

    LIQUID BLENZ CORP is recalling Pure Shilajit Tonic due to potential under-processing that could allow Clostridium botulinum growth. The product may also contain unlawful health claims.

    Product
    Pure Shilajit Tonic 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0541-2026·2026-05-27

    Liraglutide Injection Recalled Due to Particulate Matter in Cartridges

    Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.

    Product
    LIRAGLUTIDE — LIRAGLUTIDE (LIRAGLUTIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2229-2026·2026-05-27

    Integris-Allura X-ray systems with degraded deaeration hoses recalled

    Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.

    Product
    Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0846-2026·2026-05-27

    Ghirardelli Premium Hot Cocoa Mix Recalled for Salmonella Contamination

    Ghirardelli Chocolate Company is recalling Premium Hot Cocoa Mix due to potential Salmonella contamination. Affected lots were distributed throughout the U.S. and internationally.

    Product
    GHIRARDELLI PREMIUM HOT COCOA MIX NET WT 32oz (2lbs) 907g Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620126
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-2204-2026·2026-05-27

    Swan-Ganz Pacing Catheter Model D200F7 Recall Due to Leak Risk

    Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.

    Product
    Swan-Ganz Pacing Catheter, Models: D200F7;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2026·2026-05-27

    Medtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier

    Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide