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.

15851–15875 of 20371

  • HighFDA (Drugs)·D-1365-2022·2022-08-31

    Sunscreen Products Recalled Due to Improper Storage Temperature Conditions

    Family Dollar Stores is recalling multiple sunscreen products that were stored outside appropriate temperature conditions. The storage deviation may have reduced the products' sun protection effectiveness.

    Product
    BANANA BOAT SPRT CLR SPRY SPF50 6 FL OZ SKU 2007524 SUNTONE SPORT SPRAY SPF 50 5.5 OZ SKU 2096102 HAWAIIAN TROPIC TANNING OIL SPRAY PUMP SPF 25 8 FL OZ SKU 2096111 BANANA BOAT SPORT ULTRAMIST SPRAY SPF 65 6 OZ SKU 2096117 COPPERTONE WATERBABIES LOTION SPF 50 8 FL OZ SKU 20
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1562-2022·2022-08-31

    Enjoy Life and Trader Joe's Soft Baked Cookies Recalled for Hard Plastic Pieces

    Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Cookies (Snickerdoodle) and Trader Joe's Soft-Baked Snickerdoodles due to potential hard plastic pieces in the products. Consumers should not eat affected packages.

    Product
    Enjoy Life Soft Baked Cookies Snickerdoodle, 6 oz .(170g) UPC 853522000184 Trader Joe's Soft-Baked Snickerdoodles, 6 oz. UPC 0094 0757
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1383-2022·2022-08-31

    FDA Recalls NPX Antibiotic Ointments for Improper Storage Temperature

    Family Dollar Stores is recalling three NPX antibiotic ointment products due to improper storage temperature conditions that may affect product quality. Consumers should return or discard the products.

    Product
    NPX TRIPLE ANTIBIOTIC OINTMENT 1 OZ SKU 910320 NPX PAIN ITCH SCAR ANTIBAC OINTMENT 1 OZ SKU 999855 NPX TRPL ANTIBIOTIC PLS PAIN OINMNT 1 OZ SKU 901498 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1588-2022·2022-08-31

    Drug screening tablets affected by temperature exposure during storage

    McKesson is recalling Alere Toxicology drug screening tablets due to temperature excursions during facility storage that may have reduced product effectiveness. Affected units were received between June and September 2021.

    Product
    Alere Toxicology TABLET, INSTANT BLUING F/DRUGSCREEN Model Number: 7875
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1620-2022·2022-08-31

    Medical disinfectant recalled due to temperature exposure during storage

    McKesson is recalling CaviCide and EnviroCide disinfectants that may have been exposed to excessive temperatures during storage from June to August 2021, potentially reducing their effectiveness.

    Product
    a. METREX RESEARCH CORP CaviCide1 DISINFECTANT, CLNR CAVICIDE1 1GL (4/CS) METREX, Model Number: 13-5000. b. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE 8OZ SPRAY MX-1008 METREX Model Number: 13-1008. c. METREX RESEARCH CORP CaviCide DISINFECTANT, CAVICIDE GL MX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2022·2022-08-31

    FDA Recalls Exacta-Mix 2400 Compounding System for Potential Valve Leaks

    Baxter Healthcare is recalling the Exacta-Mix 2400 compounding system due to potential leaking valves on ports 1-4 in certain lots. Affected units have lot numbers 60316024 and higher.

    Product
    The Exacta-Mix 2400 compounding system, manufactured by Baxter Healthcare Corporation, is a compounding device used in the pharmacy to compound multiple source ingredients into one final solution. This device is not intended for direct patient hook-up.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1607-2022·2022-08-31

    Chest Drain System Atrium 2100 mL recalled due to temperature exposure

    The GETINGE OCEAN Chest Drain System Atrium 2100 mL is being recalled due to facility temperature excursions from June-August 2021 that may have impacted product effectiveness. Affected units were distributed nationwide between June 1 and September 30, 2021.

    Product
    GETINGE USA SALES LLC OCEAN Chest Drain System Atrium 2100 mL Model Number: 2002-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1400-2022·2022-08-31

    ZzzQuil Night Pain Berry Recalled Due to Improper Storage

    ZzzQuil Night Pain Berry 12 FL OZ distributed to Family Dollar Stores from April 30 through June 10, 2022, was held outside appropriate storage temperature conditions, which may compromise medication stability and integrity.

    Product
    ZZZQUIL NIGHT PAIN BERRY 12 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1583-2022·2022-08-31

    McKesson blood coagulation test kits recalled for temperature storage damage

    McKesson recalls Coag-Sense blood coagulation test kits nationwide due to facility temperature excursions that may have affected test effectiveness.

    Product
    a. Rapid Test Kit Coag-Sense Professional Blood Coagulation Test Prothrombin Time Test (PT/INR) Whole Blood Sample 50 Tests-IVD. Part No. 0356-50. b. Coagulation Control Kit Coag-Sense PT / INR Test (Prothrombin Time Test) Low Level / High Level 10 Strips Part No. 03P69-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1567-2022·2022-08-31

    Enjoy Life Chewy Bars recalled for hard plastic pieces

    Enjoy Life Natural Brands is recalling Chewy Bars Sunseed Crunch due to potential hard plastic fragments in the product. Affected products were distributed nationwide in the US and Canada.

    Product
    Enjoy Life Chewy Bars Sunseed Crunch, 5.75 oz UPC 853522000627
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1568-2022·2022-08-31

    Enjoy Life Chewy Bars Recalled for Hard Plastic Contamination

    Enjoy Life Natural Brands is recalling Chewy Bars - Caramel Blondie due to potential hard plastic pieces. About 89,736 cases were distributed in the US and Canada.

    Product
    Enjoy Life Chewy Bars Caramel Blondie (Chocolate Chip and Caramel), 5.75 oz (165g) UPC 819597011258 and 819597011333
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1597-2022·2022-08-31

    LeadCare II Blood Lead Test Kit Recalled Due to Temperature Storage Issues

    81 kits of LeadCare II blood lead test devices were recalled because temperature exposure during storage may have impacted product effectiveness. The affected lots were received between June and September 2021.

    Product
    MAGELLAN DIAGNOSTICS LeadCare II Blood Lead Test Kit Rapid Test Kit LeadCare II General Chemistry Blood Lead Test Whole Blood Sample 48 Tests Model Number: 70-6762
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1578-2022·2022-08-31

    Baxter DISCPAC Syringe Tip Caps recalled due to sterile barrier failure

    Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because packaging may not maintain a sterile barrier. Affected units were distributed worldwide including the US, Australia, Finland, Germany, Spain, and the UK.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF H938693025, b) 100 pack REF H938673100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1570-2022·2022-08-31

    Enjoy Life Oat Breakfast Ovals Recalled for Hard Plastic Contamination

    Enjoy Life Natural Brands is recalling Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals due to potential hard plastic pieces in the product. Consumers should not consume affected items.

    Product
    Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals Chocolate Chip Banana, 8.8 oz (250g) UPC 819597012576 and 819597012705
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1626-2022·2022-08-31

    LASIK Irrigation Cannula Recalled for Potential Temperature Exposure Damage

    Beaver-Visitec medical irrigation cannulas used in LASIK eye surgery are being recalled due to storage temperature excursions. Units distributed from June through September 2021 may have reduced effectiveness.

    Product
    BEAVER-VISITEC INTERNATIONAL, INC. Visitec CANNULA, LASIK IRR (10/BX)BVRVIS Catalog #585278
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1408-2022·2022-08-31

    Witch hazel product recalled for improper storage temperature conditions

    Witch hazel product distributed to Family Dollar Stores from April through June 2022 was stored at improper temperatures. The FDA issued a Class II recall due to manufacturing and quality control (CGMP) deviations.

    Product
    TN DICKINSON WITCH HAZEL 16 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1608-2022·2022-08-31

    3M Grounding Safety Ring Pads Recalled Due to Temperature Exposure

    3M Grounding Safety Ring pads may have been exposed to excessive temperatures during storage, potentially compromising product effectiveness. The recall affects products distributed nationwide that were received between June and September 2021.

    Product
    3M COMPANY 3M PAD, GROUNDING SAFETY RING Model Number: 9165
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1602-2022·2022-08-31

    Ultrasound Probe Disinfectant Recalled: Temperature Exposure May Affect Effectiveness

    Nanosonics Sonex-HL ultrasound probe disinfectant is recalled due to temperature excursions during storage that may have affected product effectiveness.

    Product
    NANOSONICS LTD Sonex-HL Ultrasound Probe Disinfectant trophon Sonex-HL 80 mL Bottle For Trophon EPR Disinfection System Model Number: N00037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2022·2022-08-31

    Servo-air Ventilator Systems Lack Required Stability Warning Markings

    Getinge is recalling Servo-air Ventilator Systems because they lack required warning markings about stability risks when stationary. A total of 102 units were distributed in the US; 13,750 units were distributed internationally.

    Product
    Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for respiratory support, monitoring and treatment of pediatric and adult patients. Model Number: 6882000 (equipped with 6881999 mobile cart)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1443-2022·2022-08-31

    Good Sense Lice Shampoo Recalled for Improper Storage Conditions

    Family Dollar Stores recalls Good Sense Lice Shampoo 6 FL OZ distributed April-June 2022 nationwide due to CGMP deviations from improper storage temperature conditions. Products may have compromised safety or efficacy.

    Product
    GOOD SENSE LICE SHAMPOO 6FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1384-2022·2022-08-31

    Family Dollar Hydrocortisone and Cortizone Creams Recalled for Storage Deviation

    Family Dollar Stores is recalling hydrocortisone cream (1 oz, SKU 910321) and Cortizone 10 Creme (0.5 oz, SKU 910167) distributed April 30 through June 10, 2022, due to improper storage temperature conditions.

    Product
    FS HYDROCORTISONE CREAM 1 OZ SKU 910321 CORTIZONE 10 CREME 0.5 OZ SKU 910167 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1429-2022·2022-08-31

    MIRALAX 8.3 OZ Recalled Due to Improper Storage Temperature Conditions

    Family Dollar Stores is recalling MIRALAX 8.3 OZ (SKU 902219) distributed nationwide from April 30 to June 10, 2022. The product was held outside appropriate storage temperatures, violating manufacturing standards.

    Product
    MIRALAX 8.3 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1362-2022·2022-08-31

    Divalproex Sodium Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Amneal Pharmaceuticals is recalling 4,309 bottles of Divalproex Sodium Extended-Release Tablets (250 mg) due to failed dissolution specifications. The tablets may not dissolve properly, potentially affecting medication effectiveness.

    Product
    DIVALPROEX SODIUM — DIVALPROEX SODIUM (DIVALPROEX SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1454-2022·2022-08-31

    Multiple Cold and Flu Medications Recalled Due to Improper Storage Conditions

    Family Dollar Stores is recalling multiple cold and flu medications distributed April 30–June 10, 2022, because products were held outside appropriate storage temperature conditions.

    Product
    DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC NIGHT TIME CLD FLU RLF SOFT GELS 8 CT SKU 900523 ALKA SELTZER PLUS DAY NIGHT LGEL 20 CT SKU 902012 GS COLD FLU RELIEF NGHTTIME CHRY12FL OZ SKU 917523 RIC COLD FLU DAY TIME LIQUID CAP 16 CT SKU 903037 ASP SEVERE COLD COUGH CI
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1390-2022·2022-08-31

    Rubbing Alcohol Recalled for Improper Storage Temperature Conditions

    Family Dollar Stores recalled Ready In Case 50% Wintergreen Rubbing Alcohol (16 fl oz) distributed April 30–June 10, 2022 due to improper storage temperature conditions.

    Product
    READY IN CASE RUBBING ALCHL 50 PCT WNTRGRN 16 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide