The Recall Desk

State

Missouri product recalls

20,307 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.

12301–12325 of 20307

  • SevereFDA (Food)·F-1262-2023·2023-07-26

    Good & Gather Organic Frozen Cherries & Berries Recalled for Listeria Risk

    SunOpta Grains and Foods is recalling Good & Gather Organic frozen cherries and berries distributed nationwide by Target due to potential Listeria monocytogenes contamination.

    Product
    Good & Gather Organic cherries & berries fruit blend. Blueberries, dark sweet pitted cherries, tart pitted cherries & Strawberry slices. Net Wt 32 oz (2 lb) 907g, UPC 0 85239-04782 8. Keep Frozen. Distributed by Target Corporation Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2151-2023·2023-07-26

    Cardiosave Hybrid Intra-Aortic Balloon Pump recalls due to unexpected device shutdown

    Datascope has recalled Cardiosave Hybrid IABP models due to tantalum capacitor failures that may cause unexpected device shutdown, interrupting life-critical cardiac therapy.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1270-2023·2023-07-26

    Seasons Choice frozen fruit blend recalled for potential Listeria contamination

    Aldi's Seasons Choice frozen tropical fruit blend is being recalled due to potential Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Seasons Choice Tropical Blend, Pineapple, Mango, Strawberries & Papaya. Net Wt 32 oz (2lb) 907g. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2113-2023·2023-07-26

    Impella LD cardiac pump recalled for impeller damage and embolization risk

    Abiomed recalls Impella LD blood pumps due to potential interaction with aortic valve replacement devices that can damage the pump impeller and cause blood clots. Patients with these devices should contact their healthcare provider.

    Product
    Impella LD intravascular micro axial blood pump, Product Number 005082
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1265-2023·2023-07-26

    Frozen Triple Berry Blend Recalled for Potential Listeria Contamination

    Good & Gather Triple Berry Blend, sold at Target, is being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected product.

    Product
    Good & Gather Triple Berry Blend. Blueberries, Blackberries, & Red Raspberries. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04806 1. Keep Frozen. Dist By Target Corp. Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1271-2023·2023-07-26

    Seasons Choice Mixed Fruit Recalled for Potential Listeria Contamination

    Aldi's Seasons Choice Mixed Fruit is being recalled nationwide due to potential contamination with Listeria monocytogenes. Affected lot codes are FMX227603, FMX227604, and FMX227605.

    Product
    Seasons Choice Mixed Fruit, Strawberries, Pinneapple, Peaches & Mango, Net Wt 32 oz (2lb) 907g. Dist & Sold Exclusively By: Aldi, Batavia, IL 60510.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2112-2023·2023-07-26

    Impella 5.0 Blood Pump Recalled for Potential Impeller Blade Destruction Risk

    Abiomed's Impella 5.0 intravascular blood pump is recalled due to risk of impeller blade destruction when interacting with heart valve replacements. The damaged pump can cause reduced blood flow and potentially release fractured material into the bloodstream.

    Product
    Impella 5.0 intravascular micro axial blood pump, Product Number 005062
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2149-2023·2023-07-26

    Cardiosave Hybrid IABP may fail to charge batteries, interrupting therapy

    The Cardiosave Hybrid Intra-Aortic Balloon Pump may lose the ability to charge batteries in one or both bay slots, potentially interrupting critical therapy if disconnected from AC power. Low battery alarms may alert users before therapy is interrupted.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-31 0998-00-0800-32 0998-00-0800-33 0998-00-0800-34 0998-00-0800-35 0998-00-0800-45 0998-00-0800-52 0998-00-0800-53 0998-00-0800-55 0998-00-0800-65 0998-UC-0800-31* 0998-UC-0800-33* 0998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2150-2023·2023-07-26

    Intra-Aortic Balloon Pump may fail to charge batteries, interrupting therapy

    The Cardiosave Rescue Intra-Aortic Balloon Pump may lose battery charging ability in one or both bays, potentially interrupting therapy if disconnected from power. Low battery alarms may alert users before therapy stops.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1269-2023·2023-07-26

    Frozen Mixed Fruit Blend Recalled for Potential Listeria Contamination

    SunOpta's Good & Gather brand frozen mixed fruit blend is recalled nationwide due to potential Listeria monocytogenes contamination. Affected consumers should not consume this product and should return it to the retailer.

    Product
    Good & Gather Mixed Fruit Blend Pineapple Chunks, Sliced Strawberries, Mango Chunks & Sliced Peaches. Net Wt 48 oz (3lb) 1.36kg. UPC 0 85239-04821 4. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1254-2023·2023-07-26

    Trader Joe's Organic Tropical Fruit Blend recalled for potential Listeria contamination

    Trader Joe's Organic Tropical Fruit Blend is recalled due to potential contamination with Listeria monocytogenes from pineapple ingredients. The 16 oz. bags were distributed nationwide.

    Product
    Trader Joe s Organic Tropical Fruit Blend Pineapple, Banana, Strawberry, Mango, SKU #051191, packaged in pillow bags. Each case consists of 24 bags and each bag is 16 oz. UPC on retail bag: 00511919
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2116-2023·2023-07-26

    Impella CP cardiac pump recalls due to motor housing interaction with stents

    Abiomed is recalling Impella CP with SmartAssist blood pumps due to risk of motor housing interaction with transcatheter aortic valve replacement devices, which can damage the pump's impeller blades and reduce blood flow.

    Product
    Impella CP with SmartAssist intravascular micro axial blood pump, Product Numbers 0048-0024, 0048-0045, 1000080
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2017-2023·2023-07-26

    Olympus EVIS EXERA III Bronchovideoscope Combustion Hazard Recall

    Olympus is recalling EVIS EXERA III Bronchovideoscopes nationwide due to complaints of endobronchial combustion during therapeutic laser procedures. This FDA Class I recall affects approximately 9,684 units.

    Product
    Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE, Model Numbers BF-H190, BF-Q190, BF-XT190, BF-1TH190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2152-2023·2023-07-26

    Cardiosave Rescue IABP Recalled Due to Unexpected Shutdown Risk

    Datascope Corp. is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps due to capacitor failures that may cause unexpected device shutdown. The devices may stop delivering therapy without warning.

    Product
    Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model numbers 0998-00-0800-75 0998-00-0800-83 0998-00-0800-85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2012-2023·2023-07-26

    Olympus Bronchofiberscope BF Type recalled for combustion risk during laser procedures

    Olympus bronchoscopes (Models BF-PE2 and BF-TE2) are recalled due to reports of combustion inside the airway during laser-assisted medical procedures. This is an FDA Class I recall.

    Product
    Olympus BRONCHOFIBERSCOPE BF Type, Model Numbers BF-PE2, BF-TE2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1266-2023·2023-07-26

    Good & Gather Mango Strawberry Blend recalled for Listeria contamination risk

    Target's Good & Gather Mango Strawberry Blend is being recalled nationwide due to potential Listeria monocytogenes contamination. Listeria can cause serious illness.

    Product
    Good & Gather Mango Strawberry Blend. Whole Strawberries, Mango chunks & Pineapple Chunks. Net Wt 48 oz (3lb) 1.36kg, UPC 0 85239-04803 0. Keep Frozen. Dist. By Target Corp, Minneapolis, MN 55403
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2160-2023·2023-07-26

    Medline Probe Cover Kits Recalled for Inadequate Seam Barriers

    Medline is recalling 173,449 sterile probe cover kits due to inadequate seam barriers that may compromise sterility. The affected units were distributed worldwide between December 2017 and May 2023.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) ANGIOGRAPHY DRAPE PACK, Model Number 00-400305R; b) ANGIO HOLLAND PACK-LF, Model Number DYNJ0037936C; c) ANGIO HOLLAND PACK-LF, Model Number DYNJ0037936D; d) ANGIOGRAM, Model Number DYNJ0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2188-2023·2023-07-26

    Medline Ultrasound Probe Cover Kits Recalled for Inadequate Seam Barriers

    Medline Industries is recalling ultrasound probe cover kits due to inadequate barriers at the seams. The defect may allow contaminants to reach the patient during diagnostic ultrasound procedures.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: CHN OR DAVINCI PROSTATE, Model Number DYNJ902540N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2156-2023·2023-07-26

    FDA Recalls Medline Probe Cover Kits Due to Seam Defects

    Medline is recalling probe cover kits used in diagnostic ultrasound procedures. The probe covers may have an inadequate barrier at the seams, which could compromise sterility during procedures.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) BLOCK PACK, Model Number DYNJ81722; b) PAIN BLOCK TRAY, Model Number DYNJRA0827A; c) PAIN PREP TRAY W/PROBE COVER, Model Number DYNJRA0881; d) PAIN PREP TRAY W/PROBE COVER, Model Numbe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2169-2023·2023-07-26

    Medline Ultrasound Probe Cover Kits recalled for inadequate seam barrier

    Medline is recalling 770,147 ultrasound probe cover kits worldwide due to inadequate barriers at the seams. The defect could allow contamination during diagnostic ultrasound procedures.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) FETAL SURGERY CDS-LF, Model Number CDS840214Q; b) MINOR PROCEDURE TRAY, Model Number DYNDA2418; c) CLOSUREFAST PROCEDURE PACK-LF, Model Number DYNJ0365463J; d) BARIATRIC PACK, Model Nu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2023·2023-07-26

    RET Distal Probe Recalled Due to Manufacturing Defect in DNA Sequences

    FDA recalls RET Distal Probe due to manufacturing defect where DNA sequences used in production were inverted. The defect affects 61 units distributed in California, Florida, Ohio, and South Carolina and may impact diagnostic accuracy.

    Product
    RET Distal Probe. Used in Fluorescence in situ hybridization (FISH), a laboratory technique for detecting and locating a specific DNA sequence on a chromosome.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0934-2023·2023-07-26

    Norepinephrine Injectable Recalled Due to Lack of Sterility Assurance

    SterRx recalled 2,088 bags of Norepinephrine 32 mg per 250 mL (Lot #490100) distributed nationwide due to lack of sterility assurance. The recall affects a critical care medication used in intensive care settings.

    Product
    Norepinephrine 32 mg per 250 mL (128 mcg per mL) in 0.9% Sodium Chloride, 250 mL Single Dose bag, packaged in 250 mL x 12 units per case, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-702-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2158-2023·2023-07-26

    Medline Ultrasound Probe Covers Recalled for Inadequate Seam Barriers

    Medline Industries is recalling approximately 23,938 units of sterile ultrasound probe cover kits distributed worldwide from December 2017 to May 2023 due to inadequate barriers at seams that could compromise sterility during diagnostic ultrasound procedures.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) NERVE BLOCK ACCESSORY PACK, Model Number DYNJRA1220; b) PERI NEURO BLOCK PACK-LF, Model Number DYNJRA1773; c) PERI NEURO BLOCK PACK-LF, Model Number DYNJ51107B; d) PERI NEURO BLOCK PAC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2023·2023-07-26

    Medline Ultrasound Probe Cover Kits Recalled for Defective Seam Barriers

    Medline Industries recalls probe cover kits used in diagnostic ultrasound procedures because the covers may have inadequate barriers at the seams. Approximately 3.7 million units are affected.

    Product
    Medline Probe Cover Kits containing sterile Ultrasound Gel, Labeled as the following: a) ANGIOGRAPHY PACK, Model Number DYNJ55252C; b) CATH LAB PACK, Model Number DYNJ55455A; c) CATH LAB 2, Model Number DYNJ55680A; d) IR ANGIO TRAY, Model Number DYNJ56038A; e) CATH PACK, Mod
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2153-2023·2023-07-26

    Simplexa Direct Amplification Disc Kit recalled for potential liquid spillage

    DiaSorin Molecular is recalling the Simplexa Direct Amplification Disc Kit due to potential malfunction that could cause liquid to spill from the device.

    Product
    Simplexa Direct Amplification Disc Kit, Rx Only, IVD The Simplexa Direct Amplification Disc Kit, REF: MOL1455 is 1 box containing 3 Direct Amplification Discs (DADs). Each box contains discs individually pouch-sealed and labeled with REF: MOL1452
    Category
    Medical Device
    Distribution
    Distributed nationwide