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.

26126–26150 of 50450

  • HighFDA (Drugs)·D-1107-2019·2019-04-17

    FDA Recalls Compounded Papaverine-Phentolamine-PGE1 Injectable Due to Insanitary Conditions

    FDA is recalling compounded Papaverine-Phentolamine-PGE1 injectable vials from Professional Compounding Pharmacy due to insanitary conditions observed during compounding.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 30-1 MG-20 MCG/ML* INJECTABLE, 5 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .
    Category
    Drug
    Distribution
    1 state
  • HighNHTSA·19E029000·2019-04-15

    Triumph Recalls Thruxton Motorcycles Due to Wiring Clearance Issue

    Triumph is recalling 2016-2018 Thruxton motorcycles because accessory fairing kits may damage wiring, causing loss of lights or engine stalls.

    Product
    TRIUMPH — TRIUMPH THRUXTON 1200R, THRUXTON 1200, THRUXTON A2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19103·2019-04-11

    DICK'S Recalls Field & Stream Tree Stands Due to Fall Hazard

    DICK'S Sporting Goods is recalling Field & Stream Timberline Hang On tree stands because the seat weld can break, posing a fall hazard.

    Product
    Field & Stream Timberline Hang On tree stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19104·2019-04-11

    Specialized Recalls Bicycles with Steerer Tube Collars Due to Fall Hazards

    Specialized is recalling about 63,000 bicycles because the steerer tube collar can crack, causing sudden loss of steering control and posing fall and injury hazards.

    Product
    Specialized Roubaix, Ruby, Diverge, and Sirrus Bicycles with steerer tube collars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1229-2019·2019-04-10

    Willamette Valley Frozen Strawberries Recalled for Hepatitis A Risk

    Willamette Valley Pie Company is recalling 1,448 cases of frozen strawberries due to potential Hepatitis A virus contamination. The product was distributed in California, Oregon, Texas, and Washington.

    Product
    Frozen IQF Strawberries packed in a flexible polybag. Each bag is 2 lbs (906.5g), 6 bags per case. UPC is UPC: 0 22518 87710 3. The label of 2 lb. bag is read in parts: "***STRAWBERRIES***KEEP FROZEN***Net Weight 2 lbs. ***WILLAMETTE VALLEY FRUIT ***". The white…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1235-2019·2019-04-10

    Better Made Potato Chips Recalled for Undeclared Milk

    Better Made Snack Foods is recalling 660 bags of Original Potato Chips due to undeclared milk. The product was sold in Michigan, Ohio, and via mail order nationwide.

    Product
    Better Made Snack Foods Family Size $3.99 Original Potato Chips 10oz. flexible pouch bag UPC code of 041633063048 12 bags per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V287000·2019-04-10

    2019 Jeep Renegade and Fiat 500X Recalled for Software Defect

    Chrysler is recalling 2019 Jeep Renegade and Fiat 500X vehicles because incorrect software may disable passive safety features, increasing injury risk in a crash.

    Product
    JEEP — JEEP, FIAT RENEGADE, 500X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V286000·2019-04-10

    Spartan Recalls 2012-2018 Utilimaster Reach Vehicles for Wiper Defect

    Spartan Motors is recalling 2012-2018 Utilimaster Reach vehicles because improper electrical grounding may cause windshield wipers to stop working, reducing visibility.

    Product
    UTILIMASTER — UTILIMASTER REACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1087-2019·2019-04-10

    Zimmer Biomet Recalls RingLoc Hip System Self-Tapping Bone Screws

    Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws due to a potential packaging error where 30mm screws may be labeled as 20mm and vice versa.

    Product
    Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile Titanium, Accessory to total hip implant Item Number: 103533 Product Usage: Accessory to total hip implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1232-2019·2019-04-10

    Century Snacks Recalls Honey Bliss Nut Mix for Undeclared Milk Allergen

    Century Snacks LLC is recalling Snak Club Honey Bliss Nut Mix because the Honey Butter Seasoning contains milk, a major allergen, that was not declared on the packaging.

    Product
    Snak Club Honey Bliss Nut Mix: Honey Butter Flavored Almonds, Peanuts, Pumpkin Seeds, Pistachios, Pecans & Honey Sesame Sticks. NET WET,3-oz. and 5.75-oz plastic pouches and 25 lb. bulk bags 3 oz. UPC: 0 87076 21152 3, 5.75 oz. UPC: 0 87076 51152 4
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-1086-2019·2019-04-10

    Zimmer Biomet Recalls RingLoc Hip System Bone Screws Due to Packaging Error

    Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws because 30mm screws may have been packaged as 20mm screws, and vice versa.

    Product
    Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant Item Number: 103531 Product Usage: Accessory to total hip implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1081-2019·2019-04-10

    Biomet Cement Plug Inserter Recalled for Sterilization Validation Issues

    Zimmer Biomet is recalling 89 units of the Small Diameter Cement Plug Inserter due to a lack of adequate sterilization validation.

    Product
    Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical procedures utilizing the Small Diameter Cement Plug implant devices Item Number: 414989
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1078-2019·2019-04-10

    Beckman Coulter Recalls UniCel DxC Clinical Systems Due to Software Error

    Beckman Coulter is recalling UniCel DxC clinical systems where a software scheduling error can cause sample mishandling and generate incorrect test results.

    Product
    UniCel DxC 660i, 680i, 860i, and 880i SYNCHRON Access Clinical Systems, that are re-configured so that the DxI system is separated from the DxC system and the DxI instrument is then connected to an automation line. System Name/ Catalog Number: DxC 660i/ A64871, DxC 680i…
    Category
    Medical Device
    Distribution
    26 states
  • HighNHTSA·19V285000·2019-04-10

    North Central Emergency Recalls Ambulances Due to Brake Light Wiring Defect

    North Central Emergency is recalling 2016-2018 ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    NORTH CENTRAL EMERGENCY — NORTH CENTRAL EMERGENCY, CHEVROLET FORD E-350, FORD E-450, G4500, CHEVY G4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1231-2019·2019-04-10

    Fungi Perfecti Recalls Host Defense Blood Sugar Supplement for Undeclared Wheat

    Fungi Perfecti LLC is recalling Host Defense MycoBotanicals Blood Sugar dietary supplements because they contain undeclared wheat. The recall affects 11,042 bottles distributed in the US, Canada, and Norway.

    Product
    Host Defense MycoBotanicals Blood Sugar, dietary supplement, 500mg capsules, 60 ct per bottle, serving size 2 capsules per day. UPC: 6 33422 70474 6 (distributed in US) UPC: 8 22078 71303 9 (distributed in Canada) The product is labeled in parts: "***HOST DEFENSE MYCO…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1077-2019·2019-04-10

    Morphine Sulfate API Recalled for Microbial Contamination Out of Specification

    Johnson Matthey Inc. is recalling Morphine Sulfate USP Milled API due to bioburden out of specification results.

    Product
    Morphine Sulfate USP Milled, Active Pharmaceutical Ingredient, Rx only, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1234-2019·2019-04-10

    Newport Ingredients Recalls Maika'i Sweet Honey Nut Snack Mix for Undeclared Milk

    Newport Ingredients is recalling Maika'i Sweet Honey Nut Snack Mix due to undeclared milk. The product was distributed in Hawaii.

    Product
    Maika'i Sweet Honey Nut Snack Mix, Honey Sesame Sticks, Almonds, Pumpkin Seeds, Peanuts, Pistachios & Pecans. NET WT. 8 oz. (226) clear plastic bags; UPC: 6 18551 60132 6 Packed on shared equipment with peanuts, tree nuts, wheat, soy and milk. Distributed by…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1077-2019·2019-04-10

    Beckman Coulter UniCel DxI 600 and 800 Systems Recalled for Software Error

    Beckman Coulter is recalling UniCel DxI 600 and 800 systems due to a software scheduling error that can cause incorrect immunoassay results.

    Product
    The UniCel DxI 600 and 800 Access Immunoassay Systems, that are connected to an automation line. UniCel DxI 600 Catalog Numbers: A30260, A71460, A71461, A92060. Unicel DxI 800 Catalog Numbers: 973100, A71456, A71457, A84545, A25288, A25285.
    Category
    Medical Device
    Distribution
    26 states
  • HighNHTSA·19V281000·2019-04-09

    Horton Ambulances Recalled for Reversed Backup Camera Image

    Halcore Group is recalling 2016-2019 Horton ambulances because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    HORTON — HORTON TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide