The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

34726–34750 of 50502

  • HighFDA (Food)·F-2172-2016·2016-09-21

    Mars Recalls Combos Cheddar Cheese Crackers for Undeclared Peanut Residue

    Mars Chocolate North America is recalling Combos Cheddar Cheese Crackers due to potential undeclared peanut residue.

    Product
    COMBOS SNACKS CHEDDAR CHEESE CRACKER - 15 OZ Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419780497
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2815-2016·2016-09-21

    ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak

    ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.

    Product
    Monitoring Kit with 30mL Flush Device, Item No. 46076-15 Product Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2787-2016·2016-09-21

    Howmedica Recalls AccuLIF PL Cages Due to Height Reduction

    Howmedica Osteonics Corp. is recalling AccuLIF PL Cages because some implants have shown a reduction in height greater than 1 mm after surgery.

    Product
    AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage, Rx only, Sterile R, Legal The AccuLIF PL Cages are indicated for intervertebral body fusion with autograft and/or allogeneic bone graft comprised of cancellous and/or corticocancellous bone graft when the subject device is used as an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2164-2016·2016-09-21

    Snack Factory Pretzel Crisps Recalled for Undeclared Milk Allergen

    Baptista's Bakery is recalling Snack Factory Pretzel Crisps Srircha Lime because a consumer reported the presence of seasoned product containing undeclared milk.

    Product
    Snack Factory, Pretzel Crisps Srircha Lime, UPC 049508006060, 7.2 oz(204g).
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2130-2016·2016-09-21

    Panzanella Bread Recalled for Undeclared Soy and Wheat Allergens

    Golden Crown Bakery is recalling Sourdough PAN 3 lbs. SLC Bread due to undeclared soy and wheat allergens and missing ingredient labels.

    Product
    Sourdough PAN 3 lbs. SLC Bread; No ingredient statement on label. No labeling agreement with consignees. Some of the packages list the name of the bread in the paper bag. The 3lb designation is for dough weight, not net wt. Sliced breads are individually wrapped in in…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2823-2016·2016-09-21

    ICU Medical Recalls SafeSet Reservoir and Blood Sampling Kits

    ICU Medical is recalling specific SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.

    Product
    Monitoring Kit with TP4, 30 ml Squeeze Flush and Needleless Valve, Item No. 46103-22 Usage: The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2166-2016·2016-09-21

    Mars Recalls Combos Pizzeria Pretzels for Undeclared Peanut Residue

    Mars Chocolate North America is recalling Combos Pizzeria Pretzels due to potential undeclared peanut residue. The recall covers 183,678 cases distributed nationwide and abroad.

    Product
    COMBOS PIZZERIA PRETZEL - Net Wt. 6.30 Oz. (178.6 g) Mars Chocolate North America, LLC Hackettstown, NJ 07840-1503 USA UPC 41419420065
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2117-2016·2016-09-21

    Hostess Zingers Raspberry Recalled for Unlabeled Peanut Allergen

    Hostess Brands is recalling Zingers Raspberry cakes because they were made with flour containing peanut allergen but are not labeled to contain peanuts.

    Product
    Iced Raspberry cake with creamy filling, packaged as Hostess Zingers Raspberry in 10-ct multi-packs of individual cakes, net wt. 13.40oz (360 g), UPC 888109110604; 6-ct. single serving fun size snack packs, 3 cakes per pack net wt. 4.02oz. (108g), UPC 888109010089; with the…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2138-2016·2016-09-21

    Gasco Industrial Recalls Soy Sauce Due to Undeclared Wheat

    Gasco Industrial is recalling 3,079 units of 1-gallon soy sauce sold in Puerto Rico and Saint Berthelemy because the product contains undeclared wheat.

    Product
    Label reads in part as: "Gasc¿ QUALITY BRAND***Salsa Soya (Soy Sauce)***Contenido Neto (Net Content): 1 Gal¿n (1 Gallon) (3.79 L)***GASCO INDUSTRIAL CORP. P.O. BOX 1360 GURABO, P.R. 00778 TEL. (787) 737-4000".
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·16E073000·2016-09-20

    Porsche Brake Fluid Recall Due to Missing DOT 4 Labeling

    Porsche is recalling specific 1L and 30L brake fluid containers manufactured between September 2015 and August 2016 because they lack the required 'DOT 4' label, posing a risk of incompatible fluid use.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V680000·2016-09-20

    Porsche Recalls 2017 Macan Models Due to Front Suspension Defect

    Porsche is recalling 2017 Macan models because front anti-rollbar links may move out of position, causing oversteer and increasing crash risk.

    Product
    PORSCHE — PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16267·2016-09-20

    Denon Recalls HEOS 1 Go Pack Battery Packs for Fire and Burn Hazards

    Denon is recalling HEOS 1 Go Pack rechargeable battery packs because they can overheat, posing fire and burn hazards. No injuries have been reported.

    Product
    HEOS 1 Go Pack rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V675000·2016-09-19

    Mitsubishi Recalls 2017 Mirage Vehicles for Headlight Adjustment Defect

    Mitsubishi is recalling 2017 Mirage vehicles with HID headlamps because the horizontal adjustment clips may not be secured, potentially reducing visibility or blinding oncoming drivers.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V672000·2016-09-16

    Toyota Recalls 2016 Prius Vehicles Due to Air Bag Inflation Error

    Toyota is recalling 7,817 model year 2016 Prius vehicles because a manufacturing error may cause the front passenger air bag to partially inflate unintentionally.

    Product
    TOYOTA — TOYOTA PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V671000·2016-09-16

    Jayco Recalls 2017 Octane Travel Trailers for Incorrect Tire Labels

    Jayco is recalling 2017 Octane Super Lite travel trailers because incorrect tire labels may lead to over-inflation and sudden tire failure.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V673000·2016-09-16

    Forest River Recalls 2017 Salem and Wildwood Trailers for Incorrect Tire Placards

    Forest River is recalling 2017 Salem and Wildwood recreational trailers because the Federal Placard lists incorrect tire and rim specifications, which may lead to under-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V669000·2016-09-15

    Starcraft RV Recalls 2017 AR-ONE MAXX Trailers Due to Incorrect Axle Labeling

    Starcraft RV is recalling 40 model year 2017 AR-ONE MAXX LE trailers because the Federal label incorrectly states they have two axles instead of one, creating an overload risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE MAXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16263·2016-09-15

    Bungee Chairs Recalled Due to Rivet Breakage and Fall Hazard

    Big 5 Sporting Goods is recalling Captiva Designs bungee chairs because rivets can break, posing a fall hazard. Consumers should stop using them and return them for a refund.

    Product
    Bungee chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V667000·2016-09-15

    Fiat 500 Recalled for Incorrect Spare Tire Pressure Label

    FCA US LLC is recalling 2016 Fiat 500 vehicles because the spare tire placard lists an inflation pressure exceeding the tire's maximum limit.

    Product
    FIAT — FIAT 500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V670000·2016-09-15

    2016 Mercedes-Benz and Freightliner Sprinter Seat Belt Bolt Recall

    Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because rear seat belt bolts may not be properly tightened.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2069-2016·2016-09-14

    Nature Made Adult Gummies Recalled for Possible Salmonella Contamination

    Pharmavite is recalling specific lots of Nature Made adult gummies due to possible Salmonella contamination. Consumers should check lot numbers and stop using the product.

    Product
    Nature Made(R) adult gummies Multi for Her plus Omega-3, 150 count, UPC 0-31604-04275-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2080-2016·2016-09-14

    Lysander's Spicy Bourbon Rub Recalled for Undeclared Soy and Wheat Allergens

    Geneva Foods is recalling Lysander's All Natural Spicy Bourbon Flavor Rub because it contains undeclared soy and wheat allergens and does not declare sulfites.

    Product
    Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, chicken, pork, and fish; 3.8 oz (107.7 g) foil bag, 6 units per case. Manufactured by Geneva Foods, LLC.
    Category
    Food
    Distribution
    Distributed nationwide