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 the agency’s own highest classification or reported deaths or serious injuries, 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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21126–21150 of 39673

  • SevereFDA (Drugs)·D-0564-2017·2017-03-22

    Synergy Rx Recalls Malek's Magic Plus Due to Sterility Concerns

    Synergy Rx is recalling Malek's Magic Plus prescription cream because it lacks assurance of sterility and has CGMP deviations.

    Product
    MALEK'S MAGIC PLUS (retinoic acid 0.1%, hydroquinone 6%, kojic acid 3%, hydrocortisone 1%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0585-2017·2017-03-22

    Synergy Rx Recalls Human Chorionic Gonadotropin Tablets Due to Sterility Concerns

    Synergy Rx is recalling Human Chorionic Gonadotropin tablets because the product lacks assurance of sterility and has CGMP deviations.

    Product
    HUMAN CHORIONIC GONADOTROPIN in 300IU and 500 IU TABLETS, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0565-2017·2017-03-22

    Synergy Rx Recalls LTP Ophthalmic Solution Due to Sterility Concerns

    Synergy Rx is recalling LTP (Lidocaine 10%, Tetracaine 2%, Phenylephrine 0.5%) ophthalmic solution nationwide due to lack of assurance of sterility and CGMP deviations.

    Product
    LTP (Lidocaine 10%, Tetracaine 2%, Phenylephrine 0.5%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0571-2017·2017-03-22

    Synergy Rx Supreme Bleaching Cream Recalled for Sterility Assurance Issues

    Synergy Rx is recalling Supreme Bleaching Cream due to a lack of assurance of sterility and CGMP deviations.

    Product
    SUPREME BLEACHING CREAM (Retinoic acid 0.05%, hydroquinone 6%, kojic acid 3%, Alpha Arbutin OTC 2%, Azeliac acid OTC 2%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0537-2017·2017-03-22

    Synergy Rx Recalls Fluorouracil Creams Due to Sterility Concerns

    Synergy Rx is recalling Fluorouracil creams because of a lack of assurance of sterility and CGMP deviations.

    Product
    FLUORORACIL 0.05% CREAM, FLUORORACIL 5% CREAM, FLUOROURACIL 4.9% IN CERAVE CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0522-2017·2017-03-22

    Synergy Rx Recalls Human Chorionic Gonadotropin Vials Due to Sterility Concerns

    Synergy Rx is recalling 1,809 vials of Human Chorionic Gonadotropin (HCG) because the product lacks assurance of sterility and has CGMP deviations.

    Product
    Human Chorionic Gonadotropin (HCG) 5,000 units/vial and 11,000 units/vial, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0576-2017·2017-03-22

    Synergy Rx Recalls TRI-BLEACHING CREAM HQ Due to Sterility Concerns

    Synergy Rx is recalling TRI-BLEACHING CREAM HQ because the product lacks assurance of sterility and has CGMP deviations.

    Product
    TRI-BLEACHING CREAM HQ (retinoic Acid 0.05%, Hydroquinone 6%, Fluocinolone 0.01%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1616-2017·2017-03-22

    Jerk Curry Powder Recalled for Lead Contamination

    Oriental Packing Co. is recalling specific lots of jerk curry powder because product samples and ingredients tested positive for lead.

    Product
    Hot/Spicy Jerk Curry Powder. Packaged under the names: Blue Mountain Country Hot Jamaican Jerk Curry Seasoning & Ocho Rios Spicy Jerk Curry Seasoning. Sold as 2 oz, 4 oz, 6 oz, 8 oz, 22 oz, and 5 lb.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0563-2017·2017-03-22

    Synergy Rx Recalls MALEK'S MAGIC Due to Sterility Assurance Issues

    Synergy Rx is recalling MALEK'S MAGIC prescription cream because it lacks assurance of sterility and has CGMP deviations.

    Product
    MALEK'S MAGIC (retinoic acid 0.05%, hydroquinone 6%, kojic acid 3%, hydrocortisone 1%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0541-2017·2017-03-22

    Synergy Rx Recalls Retinoic Acid Products Due to Sterility Concerns

    Synergy Rx is recalling various retinoic acid products due to a lack of assurance of sterility and CGMP deviations.

    Product
    RETINOIC ACID all strengths including 0.025%, 0.05% and 0.1% CREAM, RETINOIC ACID 0.025%/CLINDAMYCIN 1.2% GEL, RETINOIC ACID 0.025%/ HYALURONIC ACID CREAM, RETINOIC ACID 0.05%/HYALURONIC ACID CREAM, RETINOIC ACID 0.1% IN CERAVE CREAM, RETINOIC ACID POWDER 1 GRAM, RETINOIC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0579-2017·2017-03-22

    Synergy Rx Recalls Tri-Bleaching Cream Due to Sterility Assurance Concerns

    Synergy Rx is recalling Tri-Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.

    Product
    TRI-BLEACHING CREAM (Retinoic Acid 0.05%, Hydroquinone 8%, Fluocinolone 0.01%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1613-2017·2017-03-22

    J M Exotic Foods Recalls Ground Turmeric Due to Elevated Lead Levels

    J M Exotic Foods Inc is recalling specific lots of ground turmeric because a supplier sample tested with elevated lead levels. The product was distributed in Georgia and Alabama.

    Product
    Ground Turmeric packaged as follows: a) FOOD LOCKER(R) , 16 oz, PHENIX FOOD SERVICE, PHENIX CITY, AL 36867 b) Ground Turmeric, Net Wt. 4 oz.,
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0525-2017·2017-03-22

    Synergy Rx Recalls Ketoconazole and Hydrocortisone Cream Due to Sterility Concerns

    Synergy Rx is recalling all lots of Ketoconazole 2%/Hydrocortisone 1.5% Cream because the product lacks assurance of sterility and has CGMP deviations.

    Product
    KETOCONAZOLE 2%/HYDROCORTISONE 1.5% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0601-2017·2017-03-22

    Synergy Rx Recalls Intimate Bleaching Cream Due to Sterility Assurance Issues

    Synergy Rx is recalling Intimate Bleaching Cream because the product lacks assurance of sterility and has CGMP deviations.

    Product
    INTIMATE BLEACHING CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0534-2017·2017-03-22

    Synergy Rx Recalls Topical Acne Medications Due to Sterility Concerns

    Synergy Rx is recalling specific clindamycin and tretinoin products due to a lack of assurance of sterility and CGMP deviations.

    Product
    CLINDAMYCIN 1%, AZELAIC ACID 10% CREAM, CLINDAMYCIN 1.2%/ TRETINOIN 0.05% GEL, CLINDAMYCIN 1.2%/ TRETINOIN 0.1% GEL CLINDAMYCIN 2.5%, BENZOYL PEROXIDE 5%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0562-2017·2017-03-22

    Synergy Rx Recalls LP Cream Due to Sterility Assurance Issues

    Synergy Rx is recalling LP Cream (Lidocaine 15%/Prilocaine 5%) because the product lacks assurance of sterility and has CGMP deviations.

    Product
    LP CREAM (Lidocaine 15%/Prilocaine 5%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1595-2017·2017-03-22

    Bee International Recalls Plastic Heart Tubes with Chocolate Lentils

    Bee International is recalling Plastic Heart Tubes with Chocolate Lentils because they may contain undeclared milk protein.

    Product
    Plastic Heart Tubes with Chocolate Lentils, Net Wt. 1.7oz (48g), UPC 0-73563-00805-9, 24 count tubes per case
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0549-2017·2017-03-22

    Synergy Rx Recalls Lactic Acid Solution Due to Sterility Concerns

    Synergy Rx is recalling Lactic Acid Solution in all strengths due to a lack of assurance of sterility and CGMP deviations.

    Product
    LACTIC ACID SOLUTION in all strengths including 20%, 30%, and 60%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0545-2017·2017-03-22

    Synergy Rx Recalls Urea 40% Cream Due to Sterility Concerns

    Synergy Rx is recalling Urea 40% Cream because it may not be sterile and has CGMP deviations.

    Product
    UREA 40% Cream, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V191000·2017-03-21

    Isuzu Recalls NPR, NQR, and NRR Trucks for Loose Wheel Bolts

    Isuzu is recalling 2011-2017 NPR, NQR, and NRR trucks because left rear wheel bearing hub locking bolts may be loose, increasing crash risk.

    Product
    ISUZU — ISUZU NRR, NQR, NPR, NPR XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2017·2017-03-21

    J & Y Dasung Recalls Frozen Pork Dumplings Produced Without Inspection

    J & Y Dasung, Inc. is recalling approximately 178,335 pounds of frozen pork dumplings produced without federal inspection. The products were shipped to retail locations in Southern California.

    Product
    J & Y Dasung, Inc. Recalls Pork Dumpling Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·17112·2017-03-21

    Polaris Recalls Sportsman 850 and 1000 ATVs for Burn and Fire Hazards

    Polaris is recalling about 19,200 Sportsman 850 and 1000 ATVs because heat shields can melt and exhaust springs can stretch, posing burn and fire risks.

    Product
    Sportsman 850 and 1000 all-terrain vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2017·2017-03-19

    H & B Packing Recalls Boneless Beef Due To E. coli O103 Contamination

    H & B Packing Co. is recalling approximately 79,461 pounds of boneless beef products produced on March 6, 2017, due to possible E. coli O103 contamination.

    Product
    H & B Packing Co. Inc. — H & B Packing Co., Inc. Recalls Boneless Beef Products Due To Possible E. coli O103 Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V189000·2017-03-17

    BMW Recalls 2017 X5 Models Due to Air Bag Inflator Defect

    BMW is recalling 2017 X5 vehicles because the passenger air bag inflator may not vent properly, potentially causing metal fragments to strike occupants in a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide