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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35351–35375 of 39756

  • CriticalFDA (Food)·F-0932-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 951 lbs of H E B brand cold smoke salmon due to potential Listeria monocytogenes contamination.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***H E B***ALL NATURAL***SMOKED***SALMON***Sliced and Ready to Serve***4 oz***
    Category
    Food
    Distribution
    17 states
  • CriticalFDA (Food)·F-0934-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling Cold Smoke Salmon in vacuum plastic bags due to potential contamination with Listeria monocytogenes.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***Smoke***Nova***Salmon***Supreme Fine Foods*** 2lb***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Devices)·Z-0712-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Product Code: 1867-15-180 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-135-2013·2013-01-30

    Genentech Recalls Trastuzumab Kits Due to Potential Glass Particulates

    Genentech is recalling 2,140 Trastuzumab Kits for investigational use because the included Bacteriostatic Water for Injection diluent vials may contain glass particulates.

    Product
    Trastuzumab Kit containing 1 vial Trastuzumab (nominal content: 440 mg); 1 20 mL multiple dose vial Bacteriostatic Water for Injection, USP (1.1% benzyl alcohol), Manufactured by Hospira, Inc., for Genentech, Inc., South San Francisco, CA 94080-4990, NDC 50242-903-69; and 1…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0705-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screw Recall for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0708-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screw Recall for Potential Disassociation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Code: 1867-15-970 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0927-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling cold smoked salmon products due to potential contamination with Listeria monocytogenes. The recall affects specific lots distributed across multiple states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***HAND-PACKED***DARN GOOD***Atlantic Smoked Salmon***KOSHER***einsteinbros.com***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Devices)·Z-0713-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Component Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: 1867-15-199 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0919-2013·2013-01-30

    Haig's Delicacies Recalls Tzatziki for Undeclared Milk Allergen

    Haig's Delicacies is recalling Tzatziki yogurt products sold in California, Washington, and Maryland because they contain undeclared milk, wheat, and eggs.

    Product
    Tzatziki; Greek yogurt with cucumber and dill. sold in 8 oz retail and 5 lb bulk food service containers. Undeclared milk. Manufactured by Haigs Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0706-2013·2013-01-30

    DePuy Spine Recalls VIPER Polyaxial Screws Due to Potential Separation

    DePuy Spine is recalling 36 units of VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Code: 1867-15-880 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0711-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Disassociation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Product Code: 1867-15-170 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0710-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER polyaxial screws because the shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Code: 1867-15-999 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0707-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Code: 1867-15-899 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-131-2013·2013-01-30

    West-ward Recalls Propylthiouracil Tablets Due to Foreign Substance Presence

    West-ward Pharmaceutical Corp. is recalling specific lots of Propylthiouracil Tablets, USP, 50 mg because uncharacteristic spots identified as steel corrosion, degraded tablet material, and hydrocarbon oil were found.

    Product
    Propylthiouracil Tablets, USP, 50 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1480-01) and b) 1000-count tablets per bottle (NDC 0143-1480-10), Rx only, Manufactured by: West-ward Pharmaceuticals Corp. Eatontown, NJ 07724.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0921-2013·2013-01-30

    Haig's Delicacies Recalls Spanakopita for Undeclared Allergens

    Haig's Delicacies is recalling Spanakopita pastries sold in 5 lb. bulk cases because they contain undeclared wheat, milk, and eggs.

    Product
    Spanakopita; a triangular phyllo dough pastry with spinach and cheese filling. sold in 5 lb. bulk Foodservice cases. Undeclared wheat, milk and eggs Manufactured by Haig's Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-130-2013·2013-01-30

    West-ward Recalls Lisinopril Tablets Due to Foreign Substance Presence

    West-ward Pharmaceutical Corp. is recalling specific lots of Lisinopril Tablets, USP 40 mg, because uncharacteristic black spots were found in the tablets.

    Product
    Lisinopril Tablets, USP 40 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1270-01); b) 1000-count tablets per bottle (NDC 0143-1270-10); Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724; and c) 1000-count tablets per bottle (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0915-2013·2013-01-30

    Wegmans Recalls Organic Spinach and Spring Mix Due to E. coli Risk

    Wegmans is recalling 5 oz and 11 oz packages of Organic Spinach and Spring Mix Blend because the product may be contaminated with E. coli O157:H7.

    Product
    Wegmans Organic Spinach & Spring Mix --- Product is packaged in clam shell in two sizes: 5oz and 11oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0922-2013·2013-01-30

    Haig's Delicacies Recalls Tyropita Pastries Due to Undeclared Allergens

    Haig's Delicacies is recalling Tyropita pastries because they contain undeclared wheat, milk, and eggs. The products were distributed in California, Washington, and Maryland.

    Product
    Tyropita; a triangular phyllo dough pastry with cheese filling. sold in 5 lb. bulk Foodservice cases . Undeclared wheat, milk and eggs. Manufactured by Haig s Delicacies, Hayward, CA.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0928-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling cold smoked salmon due to potential Listeria monocytogenes contamination. The product was distributed across 17 states and Puerto Rico.

    Product
    Cold Smoke Salmon in vacuum plastic bags. Food Service Whole Smoked Side. Labeled in part: ***Unsliced Cold Smoked*** Salmon Fillet Skin On***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-0931-2013·2013-01-30

    Marine Harvest Recalls Cold Smoke Salmon for Listeria Risk

    Marine Harvest USA is recalling 4,572 lbs of Cold Smoke Salmon due to potential Listeria monocytogenes contamination.

    Product
    Cold Smoke Salmon in vacuum plastic bags, labeled in part: ***SMOKED***SALMON***Deli Sliced***Ready to Serve***Royal Fjord***Center***Cut Loin***
    Category
    Food
    Distribution
    17 states
  • SevereFDA (Food)·F-0926-2013·2013-01-30

    Marine Harvest Recalls Cold Smoked Salmon for Listeria Risk

    Marine Harvest USA is recalling 1 lb. vacuum-packed cold smoked salmon potentially contaminated with Listeria monocytogenes.

    Product
    Cold Smoke Salmon in vacuum plastic bags. Food Service Cold Smoked Salmon Trim 1 lb.
    Category
    Food
    Distribution
    17 states
  • SevereCPSC·13107·2013-01-30

    Sportspower BouncePro 14' Trampolines Recalled for Fall Hazard

    Sportspower is expanding a recall of BouncePro 14' trampolines sold at Walmart because the enclosure netting can break, posing a fall hazard.

    Product
    Sportspower BouncePro 14' Trampolines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0709-2013·2013-01-30

    DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation

    DePuy Spine is recalling VIPER Polyaxial Screws 8x80mm and larger because the screw shank may separate from the head during high-torque insertion.

    Product
    DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Product Code: 1867-15-980 Spinal Implant Component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-132-2013·2013-01-30

    West-ward Recalls Lisinopril and Hydrochlorothiazide Tablets Due to Foreign Particulates

    West-ward Pharmaceutical Corp. is recalling specific lots of Lisinopril and Hydrochlorothiazide Tablets because they contain minute stainless steel particulates.

    Product
    Lisinopril and Hydrochlorothiazide Tablets, 20 mg/25 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1264-01) and b) 1000-count tablets per bottle (NDC 0143-1264-10), Rx only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·13103·2013-01-29

    BRP Recalls Can-Am Commander Side-by-Side Vehicles Due to Fire Hazard

    BRP is recalling approximately 25,000 Can-Am Commander side-by-side vehicles because accumulated debris in the exhaust pipe area poses a fire risk.

    Product
    Can-Am® Commander Side-by-Side Off Road Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide