The Recall Desk

State

Missouri product recalls

20,364 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.

15726–15750 of 20364

  • SevereFDA (Food)·F-1653-2022·2022-09-07

    Uproot Peamilk Chocolate Recalled for Cronobacter and Botulism Risk

    Lyons Magnus is recalling Uproot Peamilk Chocolate nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 53,818,025 units.

    Product
    Uproot Peamilk Chocolate 8 fl oz. (240mL) UPC 8 60002-91544 9. Serve chilled, refrigerate after opening and use within 7 days. Manufactured for Uproot, Inc., New York, NY 10005. Sold in 18-count case UPC 10860002915446. .
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1627-2022·2022-09-07

    Milk Chocolate Protein Shake Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling approximately 53.8 million units of MRE Milk Chocolate Protein Shake nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    MRE Milk Chocolate Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57391 6. 4-count case UPC 810044573947. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1659-2022·2022-09-07

    Rejuvenate Muscle Health+ chocolate drink recalled nationwide for bacterial pathogens

    Lyons Magnus, Inc. is recalling Rejuvenate Muscle Health+ Chocolate, a nationwide distributed ready-to-drink beverage, due to findings and potential presence of Cronobacter sakazakii and Clostridium botulinum.

    Product
    Rejuvenate Muscle Health+ Chocolate 11 fl oz. (330mL). UPC 6 29046-50401 5. Serve Cold, shake well. Manufactured exclusively for Element Nutrition, Ltd., 1887 Whitney Mesa Dr. #6020, Henderson, NV 89014. 4-count wrap UPC 629046544011.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1633-2022·2022-09-07

    Sysco Imperial Med Plus Nutritional Drink Recalled for Bacterial Contamination

    Sysco Imperial Med Plus NSA 1.7 Vanilla Nutritional Drink has been recalled nationwide due to findings and potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume the product.

    Product
    Sysco Imperial Med Plus NSA 1.7 Vanilla Nutritional Drink. High Calorie, High Protein. Mildly Thick Nectar Consistency. 32 FL OZ (1 QT) 946mL UPC 7 34730-31074 9. Reorder # 0794018. 12 count case UPC 10734730310746. Refrigerate prior to serving. Shake well. Refr
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1669-2022·2022-09-07

    Kate Farms Nutrition Shake recalled nationwide for pathogenic contamination

    Kate Farms Nutrition Shake is recalled nationwide due to findings of Cronobacter sakazakii and Clostridium botulinum. The recall covers multiple lot codes with best-by dates spanning September 2022 to January 2023.

    Product
    kate farms Nutrition Shake, Vanilla. 11 fl oz (325 mL) UPC 8 11112-03058 4. 12 count case UPC 00811112030591. Shake Well. After opening, refrigerate and use within 4 days. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1612-2022·2022-09-07

    Lyons Ready Care Thickened Dairy Drink Recalled for Bacterial Contamination

    Lyons Magnus is recalling Lyons Ready Care Thickened Dairy Drink nationwide due to findings and potential for Cronobacter sakazakii and Clostridium botulinum contamination.

    Product
    Lyons Ready Care Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Grade A Made with 2% Milk Fat Milk, Vitamins A & D Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 45796-10044 2. Item 10044. 24 count case UPC 1004
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1658-2022·2022-09-07

    Protein Drink Recalled for Potential Cronobacter and Botulinum Contamination

    Lyons Magnus recalls Rejuvenate Muscle Health+ Vanilla nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume affected products.

    Product
    Rejuvenate Muscle Health+ Vanilla. 11 fl oz. (330mL) UPC 6 29046-50402 2. Serve Cold, shake well. Manufactured exclusively for Element Nutrition, Ltd., 1887 Whitney Mesa Dr. #6020, Henderson, NV 89014. 4-count Case UPC 629046544028.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1625-2022·2022-09-07

    Premier Protein Cafe Latte Shakes Recalled for Pathogenic Bacteria

    Premier Nutrition is recalling Premier Protein Cafe Latte shakes distributed nationwide due to contamination findings with Cronobacter sakazakii and Clostridium botulinum bacteria. Over 53 million units are affected.

    Product
    Premier Protein Cafe Latte High protein shake. 11 FL OZ (325mL). Packaged in the following configurations: 1. Carton UPC 6 43843-71668 6 packed in 4 count wrap UPC 643843716679. 2. Carton UPC 6 43843-71665 5 packed in 18 count case UPC 643843718567. Shake Well
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1673-2022·2022-09-07

    Oatly Oat-Milk Barista Edition recalled for potential bacterial contamination

    Lyons Magnus is recalling Oatly Oat-Milk Barista Edition (11 fl oz) nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Consumers should not consume the product.

    Product
    The Original Oatly! Oat-Milk Barista Edition. 11 fl oz (330ml). UPC 1 90646-63012 6. 18 count case UPC 20190646630120. Once opened, store in refrigerator and consume within 7 days. Distributed by: Oatly Inc., New York, NY 10017.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1670-2022·2022-09-07

    Kate Farms Nutritional Formula Recalled for Cronobacter and Botulism Risk

    Kate Farms Standard 1.4 Cal/mL nutrition formula in 325 mL bottles is recalled nationwide due to potential Cronobacter sakazakii and Clostridium botulinum. Affected lot code 8031 has best-by date November 4, 2022.

    Product
    kate farms Standard 1.4 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 11112-03001 0. 12 count case UPC 00811112030027. Shake Well. A ready-to-use oral and tube feeding formula. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 9370
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1608-2022·2022-09-07

    Intelligentsia Oat Latte recalled nationwide due to potential bacterial contamination

    Intelligentsia Oat Latte is recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products have lot codes 7112 (01/04/2023) and 8112 (01/05/2023).

    Product
    Intelligentsia, Oat Latte. Cold Coffee + Oat Milk. Net 10.9 fl oz (325 mL) Tetra Pak container UPC 8 00222-00097 6. Refrigerate after opening. Produced for: Intelligentsia Coffee, Inc., Aloha, Chicago, IL 60612.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1629-2022·2022-09-07

    MRE Vanilla Protein Shake Recalled for Potential Bacterial Contamination

    Lyons Magnus is recalling MRE Vanilla Protein Shake nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.

    Product
    MRE Vanilla Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57390 9. 4-count case UPC 810044573954. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1616-2022·2022-09-07

    Lyons Barista Style Coconut Beverage recalled for potential bacterial contamination

    Lyons Magnus is recalling Barista Style Coconut, a plant-based milk beverage, nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.

    Product
    Lyons Barista Style Coconut, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10082 4. 12 count case UPC 10045796101798. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1628-2022·2022-09-07

    MRE Salted Caramel Protein Shake Recalled for Cronobacter and Botulinum Risk

    Lyons Magnus recalls MRE Salted Caramel Protein Shake nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. Consumers should not consume affected products.

    Product
    MRE Salted Caramel Protein Shake. Whole Food Protein High protein shake. 11 FL OZ (325mL) Tetra Pak. UPC 8 10044-57392 3. 4-count case UPC 810044573930. Refrigerate after Opening. Distributed by: Redcon1, LLC, 701 Park of Commerce Blvd, Boca Raton, FL 33487
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1684-2022·2022-09-07

    Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.

    Product
    Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital setti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2022·2022-09-07

    Radiographic imaging system may exceed radiation dose limits in biplane mode

    Canon Medical's Alphenix i imaging systems may deliver radiation dose rates exceeding acceptable limits during biplane fluoroscopic procedures. Sixteen systems nationwide with software versions 8.0, 9.0, or 9.2 and TFP 1200C detector are affected.

    Product
    INFX-8000V. For radiographic and fluoroscopic studies and intervention.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1685-2022·2022-09-07

    Sucrose solution vials recalled nationwide for contamination and leaking

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to reports of leaking containers and contamination with black liquid and particulates. The product is used in hospital settings including neonatal intensive care units.

    Product
    Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital setting
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V555000·2022-09-07

    2021 Nissan Rogue Sport Seat Belt Retractor Safety Defect Recall

    Nissan is recalling 2021 Rogue Sport vehicles because seat belt automatic locking retractors may deactivate prematurely, reducing protection for child safety seats and violating federal crash protection standards.

    Product
    NISSAN — 2021 NISSAN ROGUE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1563-2022·2022-09-07

    Philips Radiography System Firmware Defect Risks Incorrect Radiation Dose

    Philips DigitalDiagnost C50 1.1 radiography systems contain a firmware defect in the Wallstand VS2 board that may cause incorrect radiation dose and anatomic marker misalignment. Eleven affected systems were distributed nationwide.

    Product
    DigitalDiagnost C50 1.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1468-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions

    Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V554000·2022-09-07

    2021 BMW X2 Seat Belt Retractor Defect Increases Injury Risk

    BMW is recalling certain 2021 X2 vehicles because the passenger seat belt retractor may deactivate early, failing to comply with federal safety standards. The defective retractor could increase injury risk in a crash.

    Product
    BMW — 2021 BMW X2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1647-2022·2022-09-07

    Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure

    Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.

    Product
    Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1648-2022·2022-09-07

    Siemens Dimension Vista CA 15-3 Diagnostic Cartridges Recalled for Measurement Bias

    Siemens Healthcare Diagnostics is recalling Dimension Vista CA 15-3 Flex reagent cartridges because the diagnostic test can produce inaccurate results, reading 26–33% lower than actual values, potentially delaying appropriate patient treatment decisions.

    Product
    Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN)/Ref Catalog Number : 10464344/K6456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1682-2022·2022-09-07

    Sweetums Sucrose Solution Recalled for Contamination and Leaking Cups

    Clinical Innovations is recalling Sweetums 24% Sucrose Solution used in NICU settings due to leaking cups and black particulates in the solution. The recall affects 1,773 boxes distributed nationwide.

    Product
    Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged in 15 mL cups with foil lid. Each cup contains 15 mL of USP purified water, 24% sugar, citric acid (buffer). Cup is latex-free, DEHP-free, BPA-fr
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2022·2022-09-07

    ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents

    Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.

    Product
    ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
    Category
    Medical Device
    Distribution
    Distributed nationwide