The Recall Desk

State

Missouri product recalls

73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,501
Critical
1,339
Severe
2,204
Most recent
2026-11-04

Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45326–45350 of 82318

  • HighFDA (Devices)·Z-0099-2018·2017-11-22

    Zimmer Biomet Recalls ROSA Surgical Devices Due to Observed Instability

    Zimmer Biomet is recalling 53 ROSA Surgical Devices because of observed instability. The devices are computer-controlled arms used in neurosurgery.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V752000·2017-11-22

    Entegra Recalls 2010-2011 RVs Due to Fire Extinguisher Defect

    Entegra is recalling 2010-2011 Aspire, Anthem, and Cornerstone RVs because the installed fire extinguishers may clog, require excessive force to activate, or have nozzles that detach.

    Product
    ENTEGRA — ENTEGRA ASPIRE, CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18703·2017-11-22

    Goal Zero Recalls Solar Charging Stations Due to Impact Hazard

    Goal Zero is recalling Street Charge solar powered charging stations because a weld failure could cause the top post to fall, posing an impact hazard.

    Product
    Street Charge solar powered mobile device charging stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E071000·2017-11-22

    Prevost Recalls Commercial Bus Driver Seats Due to Stuck Seat Belt Buckles

    Prevost is recalling specific aftermarket commercial bus driver seats because the seat belt buckle may be stuck in the locked position, preventing the seat belt from latching.

    Product
    SEAT BELTS:FRONT:BUCKLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0338-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Almonds nationwide and in Bermuda because the product contains undeclared milk.

    Product
    Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V765000·2017-11-22

    KME Fire Trucks Recalled for Pressure Valve Defect

    KME is recalling 74 fire trucks because corroding rings may cause pressure relief valves to open, reducing water pressure for firefighting.

    Product
    KME — KME PREDATOR PANTHER AERIAL, PREDATOR SS TANKER, PREDATOR SS PUMPER, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0342-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Turbinado Almonds with Sea Salt because the product contains undeclared milk. The recall affects 1,128 units distributed nationwide and in Bermuda.

    Product
    Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : 7 oz. Plastic Cup Packaged under the following: Aurora Brand and Store Branded Labeling Include: Gourmet Garage, Lee's Supermarket
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2018·2017-11-22

    ICU Medical Recalls Plum 360 Infusion Systems Due to Software Malfunction

    ICU Medical is recalling 21,461 Plum 360 Infusion Systems because a software defect can prevent users from stopping the pump or restarting delivery under specific conditions.

    Product
    Plum 360 Infusion System, List number 30010.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0340-2018·2017-11-22

    Aurora Dark Chocolate Cranberries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cranberries because the product contains undeclared milk, a major food allergen.

    Product
    Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup 4.75 oz. Plastic Pouch 9 oz. Plastic Cup 9 oz. Plastic Pouch 11 oz. Square Plastic Tub 18 oz. Family Size Plastic Pouch 26 oz. Plastic Tray Aurora Brand and Store Branded Labeling Include: AG…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V751000·2017-11-22

    Cruiser RV Recalls Vehicles with Defective Kidde Fire Extinguishers

    Cruiser RV is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog or have nozzles detach, posing injury risks during a fire.

    Product
    CRUISER RV — CRUISER RV MPG, LIBERTY, LAND ROAMER, FUN FINDER XTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V758000·2017-11-22

    Thor Motor Coach Recalls RVs with Defective Kidde Fire Extinguishers

    Thor Motor Coach is recalling 2003-2018 recreational vehicles equipped with specific Kidde fire extinguishers that may clog or detach, increasing injury risk during a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, FOUR WINDS DUTCHMEN, VENTURA, TUSCANY XTE, FREEDOM ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V755000·2017-11-22

    Keystone Recalls Recreational Trailers with Defective Kidde Fire Extinguishers

    Keystone RV is recalling 2003-2018 Crossroads, Dutchmen, and Keystone trailers because the installed Kidde fire extinguishers may clog or detach, posing injury risks during a fire.

    Product
    CROSSROADS — CROSSROADS, KEYSTONE, DUTCHMEN LONGHORN, LIL CABIN, ICE SEEKER, HILL COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V756000·2017-11-22

    Forest River and Coachmen Recalling RVs with Defective Fire Extinguishers

    Forest River is recalling 2003-2018 motorhomes and trailers equipped with certain Kidde fire extinguishers that may clog or detach, increasing injury risk during a fire.

    Product
    CONTINENTAL CARGO — CONTINENTAL CARGO, CARGO MATE, FOREST RIVER CONTINENTAL CARGO, CARGO MATE, CHARLESTON, BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0341-2018·2017-11-22

    Aurora Dark Chocolate Coffee Beans Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Coffee Beans in various package sizes due to undeclared milk. The recall covers products distributed nationwide and in Bermuda.

    Product
    Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plastic Pouch 8.25 oz. Plastic Pouch 8.25 oz. Plastic Cup 17 oz. Family Size Plastic Pouch Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market, Deciccos, Grauls Market…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0103-2018·2017-11-22

    Terumo BCT Bone Marrow Procedure Pack Recall for Labeling Errors

    Terumo BCT is recalling specific bone marrow procedure packs because patient labels contain incorrect lot numbers, catalog numbers, and expiry dates.

    Product
    HARVEST(R) TERUMOBCT, BMAC-30-07 Bone Marrow Procedure Pack, Private Practice / Clinical Use Only, REF 51416, Rx Only, STERILE EO
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0104-2018·2017-11-22

    Terumo BCT Recalls Bone Marrow Procedure Packs Due to Labeling Errors

    Terumo BCT is recalling 281 bone marrow procedure packs because the patient labels contain incorrect lot numbers, catalog numbers, and expiration dates.

    Product
    HARVEST(R) TERUMOBCT, BMAC2-120-01Bone Marrow Procedure Pack, REF 51423, Rx Only, STERILE EO
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Food)·F-0372-2018·2017-11-22

    Performance Food Group Recalls Pasteurized Crabmeat Due to Temperature Abuse

    Performance Food Group is recalling specific cans of Chicken of the Sea and Jack's Catch pasteurized crabmeat due to potential temperature abuse during transit.

    Product
    Chicken of the Sea Pasteurized Crabmeat Lump Blend, Item #411820; Chicken of the Sea Pasteurized Crabmeat Claw, Item #370810; Jack's Catch Pasteurized Crabmeat Jumbo Lump Item #193980; Jack's Catch Pasteurized Crabmeat Lump, Item #199830. All packaged in 1 LB or 16 OZ tin cans.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0079-2018·2017-11-22

    Fagron Recalls Estriol Compounding Powder Due to Quality Assurance Deviations

    Fagron, Inc. is recalling Estriol for prescription compounding due to lack of quality assurance at the API manufacturer.

    Product
    Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3) and d) 100 G bottle (NDC 51552-1392-5), Rx only, Distributed by Fagron, Inc., 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0097-2018·2017-11-22

    Smith & Nephew Recalls Intertan 10S Orthopedic Nails Due to Assembly Error

    Smith & Nephew is recalling 17 units of Intertan 10S orthopedic nails because the set screw was inserted upside down during manufacturing.

    Product
    smith&nephew TRIGEN INTERTAN 10S, REF 71675384, 10 MM X 18 CM NAIL, 130o (degrees), SET SCREW PREASSEMBLED IN NAIL
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0098-2018·2017-11-22

    Karl Storz Recalls Mislabeled High Flow Insufflation Tubing Pouches

    Karl Storz Endoscopy is recalling 496 boxes of High Flow Insufflation Tubing because some inner pouches are mislabeled with the wrong catalog number.

    Product
    STORZ High Flow Insufflation Tubing (with filter), Catalog #20400161S/10 (outer box label), ENDOFLATOR 26-430520-1 also referenced on outer box), individually packaged in a sterile pouch (Catalog #20400161S), 10 pouches per cardboard box. Some of the pouches inside of cardboard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0074-2018·2017-11-22

    Amerisource Recalls Enalapril Maleate Tablets Due to Stability Failures

    Amerisource Health Services is recalling Enalapril Maleate Tablets, 5 mg, because the product failed stability specifications.

    Product
    Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC: 68084-390-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0077-2018·2017-11-22

    Allergan Recalls Combigan Eye Drops Due to Failed Impurity Specifications

    Allergan is recalling 715,041 bottles of Combigan ophthalmic solution because the product failed impurities and degradation specifications.

    Product
    COMBIGAN — COMBIGAN (BRIMONIDINE TARTRATE, TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0075-2018·2017-11-22

    Genzyme Recalls Clolar Injection Due to Missing Package Insert

    Genzyme Corporation is recalling Clolar (clofarabine) injection vials because the package insert is incorrect or missing.

    Product
    Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection, for intravenous use, Rx Only, Mfd. by: Teva Pharmachemie Swensweg 5 Haarlem, The Netherlands Mfd. for: Genzyme Corporation, Cambridge, MA 02142, NDC 0024-5860-01.
    Category
    Drug
    Distribution
    Distributed nationwide