The Recall Desk

State

Missouri product recalls

73,478 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,496
Critical
1,344
Severe
2,198
Most recent
2026-10-14

Of the 8,496 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,198 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22001–22025 of 81974

  • SevereFDA (Drugs)·D-1157-2022·2022-06-22

    Artri King Tablets Recalled Due to Undeclared Diclofenac

    Artri King Reforzado con Ortiga Omega 3 Tablets are being recalled for containing undeclared diclofenac and being marketed without FDA approval. The recall affects 1,308 bottles distributed nationwide.

    Product
    Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1211-2022·2022-06-22

    Drager SafeStar 55 Medical Devices Recalled for Possible Filter Occlusion

    Draeger Medical is recalling approximately 35,950 Drager SafeStar 55 medical devices due to a manufacturing error that may cause occlusion of the device's filters, potentially preventing proper device function.

    Product
    Drager SafeStar 55, Catalog No. MP01790
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1375-2022·2022-06-22

    Marketside Gouda Bacon Green Chile Dip recalled due to metal contamination

    Morski Brands is recalling Marketside Gouda Bacon Green Chile Dip distributed nationwide by Walmart due to potential metal fragments in the product. Consumers should not consume affected units.

    Product
    Marketside Gouda Bacon Green Chile Dip, Net Wt 12 oz. (340 g) Keep Refrigerated UPC 6 81131 42871 2. Distributed by Walmart, Inc. Bentonville, AR 72716
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1265-2022·2022-06-22

    GE CARESCAPE Central Station power supply failure recall

    GE Healthcare is recalling CARESCAPE Central Station V2 patient monitoring devices due to potential power supply failure that can cause device shutdown and loss of patient monitoring.

    Product
    CARESCAPE Central Station (CSCS) V2, Model numbers 2082278-001 and 2082279-001. Update 3/10/2023: The following FRU and display part numbers have been added as affected devices: (1) Part #2082294-001, FRU MP200 POWER SUPPLY ASSEMBLY; (2) Part #2082293-002-R, FRU MP200 CPU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1147-2022·2022-06-22

    Medroxyprogesterone acetate injectable vials recalled for lack of sterility assurance

    Sun Pharmaceutical is recalling 26,892 vials of medroxyprogesterone acetate injectable suspension (150 mg/mL) distributed nationwide due to lack of assurance of sterility. The affected lots expire between January and June 2023.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 25 x 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1145-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Concerns

    Sun Pharmaceutical is recalling 4,625 syringes of Medroxyprogesterone Acetate Injectable Suspension (Lot HAC1951A) due to lack of assurance of sterility. The affected medication was distributed nationwide.

    Product
    MEDROXYPROGESTERONE ACETATE — MEDROXYPROGESTERONE ACETATE (MEDROXYPROGESTERONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1143-2022·2022-06-22

    Prefilled Syringes of Medroxyprogesterone Acetate Recalled for Lack of Sterility Assurance

    Afaxys Pharma is recalling 79,339 prefilled syringes of medroxyprogesterone acetate because the manufacturer could not assure sterility. The syringes were distributed nationwide.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India Distributed by: Afaxys Pharma, LLC, Charleston, SC, 29403, USA, Product…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1259-2022·2022-06-22

    Illumina MiSeq Dx Sequencing Instruments Recalled Due to Cybersecurity Vulnerability

    Illumina is recalling approximately 1,014 MiSeq Dx sequencing instruments due to a cybersecurity vulnerability. The devices are distributed worldwide and throughout the United States.

    Product
    illumina REF DX-410-1001 Model: MiSeq Dx illumina REF 15036706 Model: MiSeq Dx illumina REF 20014053 Model: MiSeq Dx
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1126-2022·2022-06-22

    Homeopathic drug Bacillinum Pulmo recalled for manufacturing deviations

    Washington Homeopathic Products recalled Bacillinum Pulmo homeopathic drug due to manufacturing practice deviations. The Class II recall, initiated in May 2022 and terminated in May 2023, affected nationwide distribution.

    Product
    Bacillinum Pulmo, Potency: 30C, 200C, Liquid Pellets, Rx only, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2022·2022-06-22

    Medtronic Cobalt ICD and CRT-D Telemetry Software Error Recall

    Medtronic is recalling Cobalt and Crome ICDs and CRT-Ds due to a software telemetry error in the CareLink SmartSync Device Manager. The error may affect device communication and remote monitoring.

    Product
    Cobalt Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Cobalt XT VR: DVPA2D1, DVPA2D4; b) Cobalt VR: DVPB3D1, DVPB3D4; c) Cobalt XT DR: DDPA2D1, DDPA2D4; d) Cobalt DR: DDPB3D1, DDPB3D4; e) Cobalt XT HF: DTPA2D4, DTPA2D1 f) Cobalt…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V441000·2022-06-22

    2023 Thomas Built Saf-T-Liner C2 School Buses Recalled for Emergency Exit Defect

    Daimler Trucks North America is recalling 2023 Thomas Built Saf-T-Liner C2 school buses because they may lack sufficient emergency exits, increasing injury risk during emergencies.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1376-2022·2022-06-22

    Dawn's Campfire BBQ Beans Recalled for Metal Foreign Object

    Morski Brands recalls 1,312 units of Dawn's Campfire BBQ Beans nationwide due to metal foreign objects. Consumers should not consume the product.

    Product
    Dawn's Campfire BBQ Beans, #90125, Net Wt 8 lb (3.63 kg) Keep Refrigerated UPC 0 32345 90125 4. Mfg By Morski Brands, Inc., Portage, WI 53901
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1146-2022·2022-06-22

    Medroxyprogesterone acetate injectable suspension recalled for lack of sterility assurance

    Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension (150 mg/mL) nationwide due to lack of assurance of sterility. Affected lots contain vials with expiration dates from December 2022 through September 2023.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Single-Dose Vial, 150 mg/mL, Rx only, Manufactured for: Northstart Rx LLC, Memphis, TN, 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol Baroda Highway, Halol-389 350, Gujarat India , NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1374-2022·2022-06-22

    Ranch BLT Pasta Salad Recalled for Metal Foreign Objects

    Morski Brands recalls Ranch BLT Pasta Salad nationwide due to possible metal fragments. The product was sold under Finest Traditions and Dawn's brands with a best-before date of 6-13-22.

    Product
    Ranch BLT Pasta Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest Traditions, Net Wt. 2/5 lbs. (10 lbs) (4.54kg), Item 10406332. UPC 10 7 33147 11722 1. Distributed By: DBC Foods, St. Cloud, MN 56302. 2. Dawn's…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1135-2022·2022-06-22

    Homeopathic drug Proteus recalled for manufacturing quality control deviations

    Washington Homeopathic Products is recalling Proteus homeopathic remedy in multiple potencies due to manufacturing process deviations. The firm initiated this voluntary recall in May 2022.

    Product
    Proteus, Potency: 7C, 8C, 9C, 12C, 15C, 16C, 20C, 30C, 200C, OTC, Liquid Pellets, Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V443000·2022-06-22

    2022 Freightliner Cascadia brake system may fail to engage

    The emergency braking system on certain 2022 Freightliner Cascadia trucks may fail to engage, creating a risk of brake failure. Dealers will install a corrective valve at no cost.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1373-2022·2022-06-22

    Steakhouse Potato Salad Recalled Due to Metal Contamination

    Morski Brands is recalling Steakhouse Potato Salad products nationwide due to metal contamination. Affected brands include Finest Traditions and Dawn's.

    Product
    Steakhouse Potato Salad, Keep Refrigerated packaged in the following brands and plastic container sizes: 1. Finest Traditions, Net Wt. 10 lb (4.54kg), Item 1038364. UPC 10-73314710773-4. Mfg By Morski Brands, Inc., Portage, WI 53801. 2. Finest Traditions, Net Wt.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1268-2022·2022-06-22

    Medtronic Crome and Cobalt Cardiac Defibrillators Recalled Due to Telemetry Error

    Medtronic recalls 3,944 Crome and Cobalt ICDs and CRT-Ds due to a potential telemetry error affecting device communication with external monitors.

    Product
    Crome Models loaded with CareLink SmartSync Device Manager application software D00U005: a) Crome VR: DVPC3D1, DVPC3D4; b) Crome DR: DDPC3D1, DDPC3D4; c) Crome HF: DTPC2D4, DTPC2D1; d) Crome HF Quad: DTPC2QQ, DTPC2Q1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1150-2022·2022-06-22

    Zileuton Extended-Release Tablets recalled for failed dissolution specifications

    Lupin Pharmaceuticals is recalling Zileuton Extended-Release Tablets, 600 mg, due to failed dissolution specifications found during stability testing that may affect medication efficacy.

    Product
    Zileuton Extended-Release Tablets, 600 mg, 120-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202 by Lupin Limited, Nagpur-441108, India, NDC 68180-169-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2022·2022-06-22

    Illumina NextSeq 550 Genetic Sequencer Cybersecurity Vulnerability Recall

    Illumina is recalling 799 NextSeq 550 Dx genetic sequencers due to a cybersecurity vulnerability in the Local Run Manager software. Affected devices have been distributed worldwide and in the United States.

    Product
    illumina Model NextSeq 550 Dx REF 20005715
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1377-2022·2022-06-22

    Finest Traditions Smokey Baked Beans recalled for potential metal contamination

    Morski Brands, Inc. is recalling 2,648 units of Finest Traditions Smokey Baked Beans due to the potential presence of foreign metal objects. The recalled product was distributed nationwide.

    Product
    Finest Traditions Smokey Baked Beans, #1038700, Net Wt 8 lb (3.63 kg) Keep Refrigerated UPC 10 7 33147 10231 9. Distributed By: DBC Foods, St Cloud, MN 56302
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V442000·2022-06-22

    2022 Grand Design Momentum Travel Trailer Electrical Fire Hazard Recall

    Grand Design is recalling 165 model-year 2022 Momentum travel trailers due to improper 110-volt electrical wiring that can overheat and create a fire risk. Dealers will rewire the power supply at no cost.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1378-2022·2022-06-22

    Potato Salad Recalled Nationwide for Metal Contamination Risk

    Morski Brands recalled 832 units of Dawn's Smoked Gouda & Bacon Potato Salad due to possible metal fragments. Consumers with products bearing best-before dates 5-13-22, 6-21-22, 6-24-22, or 6-27-22 should not consume them.

    Product
    Dawn's Smoked Gouda & Bacon Potato Salad, #10079, Net Wt 8 lb (3.63 kg) Keep Refrigerated. UPC 10032345130019. Mfg By Morski Brands, Inc., Portage, WI 53901
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1144-2022·2022-06-22

    Medroxyprogesterone Acetate Injectable Suspension Recalled for Sterility Assurance Failure

    Sun Pharmaceutical is recalling medroxyprogesterone acetate injectable suspension due to lack of assurance of sterility. The recall affects approximately 57,997 prefilled syringes distributed nationwide.

    Product
    medroxyPROGESTERone Acetate Injectable Suspension, USP, 1 mL Prefilled Syringe, 150 mg/mL, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 16714-999-01.
    Category
    Drug
    Distribution
    Distributed nationwide