The Recall Desk

State

Missouri product recalls

73,817 recalls have nationwide distribution and so reach Missouri. 8,501 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,501
Critical
1,339
Severe
2,204
Most recent
2026-11-04

Of the 8,501 recalls naming Missouri we have scored against our rubric, 1,339 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,204 (26%) are Severe.

These figures cover only the 8,501 recalls whose distribution notice names Missouri specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47326–47350 of 82318

  • ModerateFDA (Devices)·Z-2674-2017·2017-07-12

    Boston Scientific Retrieval Balloon Catheter Recalled for Incorrect Injection Labeling

    Boston Scientific is recalling 32 units of Extractor Pro RX-S Retrieval Balloon Catheters because the labels incorrectly identify the injection location relative to the balloon.

    Product
    Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter 12-15mm Below UPN: M00547340
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2673-2017·2017-07-12

    Boston Scientific Retrieval Balloon Catheter Recalled for Labeling Error

    Boston Scientific is recalling 39 units of the Extractor Pro RX-S Retrieval Balloon Catheter because the label incorrectly identifies the injection location.

    Product
    Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter 9-12mm Above UPN: M00547300
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2669-2017·2017-07-12

    Sterilmed Recalls Reprocessed EP Ablation Cables Due to Regulatory Status

    Sterilmed is recalling 963 reprocessed EP ablation cables because they are Class III devices that lack required premarket approval.

    Product
    Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The cables serve two different purposes. They either serve as an extension between an EP catheter and…
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Drugs)·D-0945-2017·2017-07-12

    G & W Clobetasol Propionate Ointment Recalled for Impurity

    G & W Laboratories is recalling Clobetasol Propionate Ointment 0.05% due to out-of-specification results for a known impurity.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0937-2017·2017-07-12

    Methocarbamol USP Recalled for Quality Assurance Deviations

    American Pharmaceutical Ingredients LLC is recalling Methocarbamol USP due to lack of quality assurance at the API manufacturer.

    Product
    Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2423-2017·2017-07-12

    Nutri-Dyn Calcium D-Glucarate Plus Recalled Due to Mislabeling

    Nutri-Dyn Midwest, Inc. is recalling 856 bottles of Calcium D-Glucarate Plus because they were mistakenly labeled as St. John's Wort during production.

    Product
    Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-2645-2017·2017-07-12

    Boston Scientific Imager II Angiographic Catheter Recall for Missing Seal

    Boston Scientific is recalling Imager II Angiographic Catheters because some units are missing the bottom pouch seal. The defect is obvious to the user.

    Product
    Boston Scientific Imager II Angiographic Catheter, a pathway for delivering contrast media to selected sites in the vascular system. M001314141 (5-pack outer package UPN), M001314140, single unit, inner package UPN)
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0944-2017·2017-07-12

    GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence

    GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.

    Product
    PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0934-2017·2017-07-12

    PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors

    PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0935-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.

    Product
    Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2659-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging

    Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0932-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0930-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0936-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.

    Product
    Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0931-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0933-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates

    PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E034000·2017-07-10

    Takata Driver Frontal Air Bag Inflator Recall for Rupture Risk

    Takata is recalling specific driver-side air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V435000·2017-07-10

    Chrysler Recalls 2011-2014 Vehicles for Alternator Failure Risk

    Chrysler is recalling specific 2011-2014 Dodge, Chrysler, and Jeep vehicles because the alternator may fail, causing the vehicle to stall or catch fire.

    Product
    DODGE — DODGE, CHRYSLER, JEEP DURANGO, 300, GRAND CHEROKEE, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V437000·2017-07-10

    GM Recalls 40,683 Vehicles for Air Bag and Seat Belt Software Defect

    General Motors is recalling 40,683 vehicles from 2014-2017 because a software error may prevent front air bags and seat belt pretensioners from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC, BUICK CORVETTE, SILVERADO 1500, SIERRA 1500, LACROSSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V438000·2017-07-10

    BMW Recalls 2014-2017 R1200GS Motorcycles for Fork Tube Separation Risk

    BMW is recalling 2014-2017 R1200GS and R1200GS Adventure motorcycles because the fixed fork tube may separate from the seal plug, increasing crash risk.

    Product
    BMW — BMW R1200 GS ADVENTURE, R 1200 GS ADVENTURE, R1200 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide