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.

15801–15825 of 20371

  • HighFDA (Drugs)·D-1431-2022·2022-08-31

    Topical Skincare Products Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling three topical skincare products distributed nationwide due to storage condition violations in manufacturing.

    Product
    ST IVES BLKHD CLRNG GREEN TEA SCRUB 6 OZ SKU 2007787 AMBI EXFOLIATING WASH 5 OZ SKU 2097153 CC BLACKHEAD SCRUB 5 OZ SKU 2032021 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 (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
  • HighFDA (Drugs)·D-1381-2022·2022-08-31

    Family Dollar Oral Pain Relief Products Recalled for Improper Storage

    Family Dollar recalled multiple oral pain relief products due to storage temperature deviations. The products were distributed to select Family Dollar stores from April 30, 2022 through June 10, 2022.

    Product
    ORAJEL GUM PAIN RELIEF GEL 0.125OZ SKU 903432 GOOD SENSE ORAL PAIN RELIEF 0.5OZ SKU 999543 ORAJEL ORAL PAIN 0.125 FL OZ SKU 912968 ORAJEL MOUTH SORE GEL 0.125 OZ SKU 999075 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    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 (Drugs)·D-1372-2022·2022-08-31

    Tylenol and Acetaminophen Products Recalled Due to Improper Storage

    Family Dollar Stores is recalling multiple Tylenol and acetaminophen products due to CGMP deviations involving improper storage temperature conditions. Products were distributed nationwide through specific Family Dollar locations from April 30, 2022 through June 10, 2022.

    Product
    Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559; TYLENOL CHILD GRAPE 4 FL OZ SKU 901600 TYLENOL CHILD ORAL SUSPENSION CHERRY 4 FO 913104 TYLENOL INFANTS DROPS DF CHERRY 1OZ SKU 999108 TYLENOL PM CAPLET 24 CT SKU 900603 TYLENOL EXTRA STRENGTH CAPLET 24 CT SKU 91698
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1401-2022·2022-08-31

    Jet Alert Tablets Recalled for Improper Storage Temperature Conditions

    Jet Alert stimulant tablets distributed nationwide from April to June 2022 are being recalled due to improper storage temperature conditions that may affect product safety and efficacy.

    Product
    JET ALERT TABLET 30 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1629-2022·2022-08-31

    Beckman Coulter Laboratory Reagents Recalled for Temperature-Related Effectiveness Loss

    Beckman Coulter diagnostic reagents used in blood analysis systems were recalled after exposure to temperature excursions during storage and shipment. Products received between June and September 2021 may have reduced effectiveness.

    Product
    BECKMAN COULTER, INC. a. COULTER DxH Diff Pack REAGENT, DIFF PK FP DXHCOULTR, Catalog #628020. b. COULTER DxH Cleaner REAGENT, CLEANER FP DXH 10LCOULTR Catalog #628023. c. DxH 500 Series Lyse LYSE, VERSA SOL DXH 500 SERIES(0.5L/KT) Catalog # B36846. d. DxH 500 Serie
    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 (Food)·F-1571-2022·2022-08-31

    Enjoy Life Breakfast Ovals Recalled for Potential Hard Plastic Pieces

    Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals (Berry Medley) are being recalled due to potential hard plastic contamination. Approximately 89,736 cases were distributed nationwide in the US and Canada.

    Product
    Enjoy Life Soft Baked Fruit & Oat Breakfast Ovals Berry Medley, 8.8 oz (250g) UPC 819597012583 and 819597012712
    Category
    Food
    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 (Devices)·Z-1592-2022·2022-08-31

    B. Braun Gravity Mixing Container Recalled for Temperature Exposure

    B. Braun EVA Gravity Mixing Container 1000 mL units may have been exposed to higher temperatures during storage prior to delivery, potentially affecting product effectiveness. Units distributed nationwide between June and September 2021 are affected.

    Product
    B. Braun EVA Gravity Mixing Container 1000 mL Model Number: 2112363
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1572-2022·2022-08-31

    Enjoy Life Brownie Bites Recalled for Potential Hard Plastic Pieces

    Enjoy Life Natural Brands is recalling Enjoy Life Brownie Bites Rich Chocolate (UPC 819597013290) due to potential hard plastic pieces in the product. No illnesses have been reported.

    Product
    Enjoy Life Brownie Bites Rich Chocolate, 4.76 oz UPC 819597013290
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1573-2022·2022-08-31

    Enjoy Life Brownie Bites recalled for potential hard plastic pieces

    Enjoy Life Natural Brands is recalling Brownie Bites - Salted Caramel (4.76 oz) due to potential hard plastic pieces. Approximately 89,736 cases were distributed nationwide in the US and Canada.

    Product
    Enjoy Life Brownie Bites Salted Caamel, 4.76 oz UPC 819597013313
    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-1621-2022·2022-08-31

    Medical Sponges Recalled for Temperature Exposure During Storage

    Mckesson Medical-Surgical is recalling MetriSponge cleaning sponges due to facility temperature excursions that may have compromised product effectiveness during storage and delivery between June and August 2021.

    Product
    METREX RESEARCH CORP SPONGE, METRISPONGE W/METRIZYME (25/BX 4BX/CS) Model Number: 10-4025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1601-2022·2022-08-31

    McKesson Colorectal Cancer Screening Tests Recalled Due to Temperature Exposure

    McKesson Medical-Surgical is recalling MMS - IMMUNOSTICS INC colorectal cancer screening test kits due to facility temperature excursions that may have reduced product effectiveness. The recall affects lots distributed between June and September 2021.

    Product
    a. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit Consult Colorectal Cancer Screening Fecal Occult Blood Test (iFOB or FIT) Stool Sample 25 Tests, Model Number: 4487. b. MMS - IMMUNOSTICS INC McKesson Rapid Test Kit McKesson Consult Colorectal Cancer Screening Fecal Occult Blo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1628-2022·2022-08-31

    Medical Lubricating Jelly Recalled Due to Temperature Excursions During Storage

    Mckesson Medical-Surgical is recalling Fisher Scientific Aseptic Control Lubricating Jelly due to temperature excursions from June–August 2021 that may have reduced product effectiveness.

    Product
    FISHER SCIENTIFIC Aseptic Control¿ LUBRICATING JELLY PAP TEST 4OZ(12/PK) Catalog #22998006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1398-2022·2022-08-31

    AZO YEAST PLUS 20 CT Recalled Due to Improper Storage Conditions

    AZO YEAST PLUS 20 CT has been recalled by Family Dollar Stores due to improper storage temperature conditions that violate CGMP requirements. The product was distributed nationwide from April through June 2022.

    Product
    AZO YEAST PLUS 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2022·2022-08-31

    Surgical Hemostatic Matrix Recalled Due to Temperature Exposure During Storage

    Mckesson is recalling Ethicon SURGIFLO Hemostatic Matrix Kit due to temperature excursions during storage that may have reduced product effectiveness. Affected units were distributed nationwide between June and September 2021.

    Product
    Ethicon SURGIFLO Hemostatic Matrix Kit with Thrombin (6/CS) Ref: 2994 Mfg: FERROSAN MEDICAL DEVICES A/S Indicated in surgical procedures (other than ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or other conventional methods is ineffective
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1590-2022·2022-08-31

    Alcon Contact Lens Solutions Recalled for Temperature Exposure During Storage and Transit

    Multiple Alcon contact lens solutions were recalled due to facility temperature excursions during storage and transit that may have reduced product effectiveness. Affected products include Clear Care and Opti Free Replenish solutions distributed nationwide between June and September 2021.

    Product
    a. Alcon Clear Care Contact Lens Solution Clear Care 12 oz. Solution, Model Number: 65035820, Model Number: USSCupA-12BUP300. b. Alcon Contact Lens Solution Opti Free Replenish 4 oz. Solution Model Number: 00065035604 Model Number: USSCupA-12BUP300. c. Alcon Contact L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1580-2022·2022-08-31

    Baxter Syringe Tip Caps Recalled Due to Sterile Packaging Barrier Risk

    Baxter Healthcare is recalling DISCPAC Syringe Tip Caps because the packaging may not maintain a sterile barrier. The product was distributed nationwide and internationally.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1595-2022·2022-08-31

    Cadwell Disposable Ground Electrodes Recalled Due to Temperature Exposure

    Cadwell Disposable Ground Electrodes may have reduced effectiveness due to facility temperature excursions between June and August 2021. All units distributed nationwide received between June 1 and September 30, 2021 are affected.

    Product
    Cadwell Disposable Ground Electrodes Grounding Pad 1.25 X 1.75 Inch Dimensions, Disposable Model Number: 302288-000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1581-2022·2022-08-31

    Baxter DISCPAC Syringe Tip Caps Recalled for Potential Sterile Barrier Failure

    Baxter is recalling DISCPAC Syringe Tip Caps due to potential packaging defect that may not maintain sterile barrier. The recall affects 8,500 units distributed worldwide.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Purple, 100 pack, REF H938677100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1575-2022·2022-08-31

    Baxter DISCPAC Syringe Tip Caps Recalled for Compromised Sterile Barrier

    Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging failure that could compromise the sterile barrier. The recall affects 602,340 units distributed worldwide.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H938690025
    Category
    Medical Device
    Distribution
    Distributed nationwide