The Recall Desk

State

Missouri product recalls

20,371 recalls have nationwide distribution and so reach Missouri. 0 additional recalls listed Missouri specifically in their distribution scope.

About recalls in Missouri

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Missouri consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

16226–16250 of 20371

  • HighFDA (Food)·F-1486-2022·2022-07-27

    Honeymoons Dark Chocolate Cashew Recalled for Undeclared Tree Nuts

    Honeymoons Dark Chocolate Cashew products may contain undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. The product is being recalled from Queen Bee retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoons Dark Chocolate Cashew. PLU Code: 788394 14864 4.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1251-2022·2022-07-27

    Epinephrine Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 134,385 epinephrine injection syringes nationwide due to lack of assurance of sterility. No illnesses have been reported.

    Product
    EPINEPHrine Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-925-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1283-2022·2022-07-27

    FDA Recalls Cipla Difluprednate Eye Drops for Defective Container Caps

    Cipla is recalling 8,136 bottles of Difluprednate ophthalmic emulsion nationwide due to defective container caps that can break and expose the medication tip, compromising sterility.

    Product
    DIFLUPREDNATE — DIFLUPREDNATE (DIFLUPREDNATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2022·2022-07-27

    Spinal Fusion Implant Cross Connectors Recalled for Insufficient Clamping Force

    Aesculap is recalling its S4 Cervical Cross Connector used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to move on the rods or shed particles.

    Product
    AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code SW112T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1468-2022·2022-07-27

    QBee Sea Salt Caramel Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.

    Product
    QBee Sea Salt Caramel. Net wt. 1 oz. PLU Code: 788394 11010 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1249-2022·2022-07-27

    Compounded Injectable Medications Recalled for Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.

    Product
    Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac Tromethamine 60 mg (1.2 mg/mL), Ketamine HCl 60 mg (1.2 mg/mL) Injection, 50 mL syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. E
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1436-2022·2022-07-27

    BD Connecta 3-Way Stopcocks Recalled Due to Potential Leakage

    Becton Dickinson recalls BD Connecta 3-Way Stopcocks due to potential leakage at the housing that may delay treatment and expose patients to biohazardous material.

    Product
    BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1488-2022·2022-07-27

    Honeymoons Milk Chocolate Pecan recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Pecan candies due to the potential presence of undeclared tree nuts. Consumers with tree nut allergies should not consume this product.

    Product
    Honeymoons Milk Chocolate Pecan. PLU Code: 788394 14684 8. Ingredients: Honey, milk chocolate (sugar, milk, cocoa butter, chocolate liquor, sunflower lecithin and pure vanilla), pecans, butter (pasteurized cream, salt) cream, nonfat dry milk, whey, sunflower lecithin, algin, a
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1276-2022·2022-07-27

    Nephron Phenylephrine HCl Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center LLC recalls Phenylephrine HCl Injection (1 mg/10 mL) syringes nationwide due to inability to guarantee sterility. Approximately 464,265 syringes across eleven lot numbers are affected.

    Product
    Phenylephrine HCl Injection, USP, 1 mg/10 mL (100 mcg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-957-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2022·2022-07-27

    Medical Device Recall: Hill-Rom PRO+ Mattress Microclimate Feature Failure

    Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.

    Product
    Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1471-2022·2022-07-27

    Honey Caramels Almond Coconut Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Almond Coconut due to potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Consumers allergic to tree nuts should not consume this product.

    Product
    Honey Caramels Almond Coconut. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz bag: 788394 12004 6. Ingredients: Honey, butter (pasteurized cream & salt), cream, almonds, coconut, nonfat dry milk, whey, natural flavors, lecithin, algi
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1460-2022·2022-07-27

    Grandma's Fudge Classic Truffle Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Grandma's Fudge Classic Truffle due to undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The product may pose a risk to individuals with tree nut allergies.

    Product
    Grandma's Fudge Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11062 7. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], sunflower lecithin & pure vanilla) honey, butter (pasteurized cream, salt), crea
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1260-2022·2022-07-27

    Ketamine HCl Injection Syringes Recalled Due to Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling Ketamine HCl Injection pre-filled syringes due to lack of assurance of sterility. The recall affects 30,745 syringes distributed nationwide.

    Product
    Ketamine HCl Injection, USP 30 mg/3 mL (10 mg/mL*) syringes, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-982-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1489-2022·2022-07-27

    Dark Chocolate Pecan Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalls Honeymoons Dark Chocolate Pecan for undeclared tree nuts including almonds, coconut, macadamia, and walnuts. The product was distributed through retail locations in CO, NM, and WY, and nationwide via internet sales.

    Product
    Honeymoons Dark Chocolate Pecan. PLU Code: 788394 14720 3.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1428-2022·2022-07-27

    Spinal Fixation Device Removal Key Recalled Due to Potential Fracture Risk

    Aesculap Implant Systems recalls ENNOVATE MIS REMOVALKEY SHORT due to fracture risk if removal key is not used at 90-degree angle. Affected units distributed in CA, CO, IL, MI, OH, and TX.

    Product
    ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1270-2022·2022-07-27

    Neostigmine Methylsulfate Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center LLC is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The recall affects 59,520 syringes distributed nationwide.

    Product
    Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL (1 mg/mL) syringe, packaged in 5 x 3 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-932-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1247-2022·2022-07-27

    Bupivacaine Injection Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 6900 syringes of Bupivacaine HCl Injection nationwide due to lack of sterility assurance. No illnesses or injuries have been reported.

    Product
    0.125% Bupivacaine HCl Injection, USP, 62.5 mg/50 mL (1.25 mg/mL) syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Ext., West Columbia, SC 29172, NDC: 69374-970-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1497-2022·2022-07-27

    Valentine Gift Box Recall Due to Undeclared Tree Nuts

    Queen Bee Gardens is recalling Valentine Gift Box products that may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Products were distributed through 10 retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Valentine Gift Box. Net wt. 7.5 oz. PLU Code: 788394 17700 2.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1463-2022·2022-07-27

    Truffle Recall: Undeclared Tree Nuts Present Allergen Risk

    Queen Bee Gardens is recalling Midnight Gold Classic Truffles for potentially containing undeclared tree nuts, which pose a risk to allergic consumers. Distribution included Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Midnight Gold Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11070 2. Ingredients: Dark chocolate, honey, butter (pasteurized cream, salt), cream, non-fat dry milk, whey, almonds, milk chocolate, natural flavor, salt, soda, agar, algin & lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1425-2022·2022-07-27

    Sensis diagnostic tool software may fail to display vital signs

    Siemens' Sensis diagnostic tool may lose communication and fail to display vital signs during initial patient exams or after inactivity. Software updates are required.

    Product
    Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model:10764561
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1415-2022·2022-07-27

    Medical Bed Mattress Microclimate Failure Increases Pressure Ulcer Risk

    Affected Hill-Rom Centrella Pro+ hospital mattresses can fail to properly manage heat and moisture removal, increasing the risk of pressure ulcer development in patients.

    Product
    Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1472-2022·2022-07-27

    Honey Caramels Blue Raspberry Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Blue Raspberry due to undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The product poses a serious risk to consumers with tree nut allergies.

    Product
    Honey Caramels Blue Raspberry. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz. bag: 788394 12675 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1494-2022·2022-07-27

    Queen Bee Gardens Chocolate Recall: Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoon Gift Box chocolates that may contain undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts.

    Product
    Honeymoon Gift Box 12 pc., 9 oz. PLU Code: 788394 96108 3 Ingredients: Dark, Milk & White Chocolate with Pecans, Cashews & Almonds
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1424-2022·2022-07-27

    Randox Cholesterol In Vitro Diagnostic Kits Fail Stated Performance Specifications

    Randox Cholesterol diagnostic kits fail to meet stated performance specifications. Calibration issues cause quality control results to fall outside acceptable ranges, potentially delaying test results.

    Product
    Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1461-2022·2022-07-27

    Queen Bee Gardens Huckleberry Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Huckleberry Truffles because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide via internet.

    Product
    Huckleberry Truffle. Net wt. 1.4 oz. PLU Code: 788394 11057 3. Ingredients: Dark chocolate (sugar, chocolate liquor processed with potassium carbonate, cocoa butter, milk fat [butter], HONEY, "Ivory" chocolate (sugar, cocoa butter, whole & non-fat milk solids, sunflower lecith
    Category
    Food
    Distribution
    Distributed nationwide