The Recall Desk

State

Missouri product recalls

72,907 recalls have nationwide distribution and so reach Missouri. 8,461 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,461
Critical
1,333
Severe
1,870
Most recent
2026-09-09

Of the 8,461 recalls naming Missouri we have scored against our rubric, 1,333 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (22%) are Severe.

These figures cover only the 8,461 recalls whose distribution notice names Missouri specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1476–1500 of 81368

  • SevereFDA (Food)·H-0909-2026·2026-06-10

    Alfredo sauce contains dry milk powder recalled over Salmonella

    Alfredo Sauce in 3 lb 7 oz sealed poly bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Alfredo Sauce, 3 lb. 7 oz., packaged in a sealed poly bag and packed 12 bags per case, UPC 0039954921963
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Devices)·Z-2254-2026·2026-06-10

    BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2252-2026·2026-06-10

    BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0981-2026·2026-06-10

    Cream cheese filled banana nut muffins do not declare walnut

    Albertsons store-made Muffins Banana Nut Cream Cheese Filled 2 count are being recalled because the contains statement does not declare walnut. Nine units are affected.

    Product
    UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1023-2026·2026-06-10

    Pad Thai chicken ready meals do not declare anchovy

    Albertsons store-made Wok Pad Thai Chicken ready meals are being recalled because the contains statement does not declare anchovy.

    Product
    UPC 21208300000 Ready Meals WOK PAD THAI CHICKEN SS COLD This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1021-2026·2026-06-10

    Albertsons grilled chicken salad does not declare almond allergen

    Albertsons store-made Kitchen Salad Grilled Chicken is being recalled because the contains statement does not declare almond. 27 units are affected.

    Product
    UPC 27163100000 Kitchen SALAD GRILLED CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2296-2026·2026-06-10

    Avanta administration tube sets may not engage the flow control valve

    Avanta Multi-Patient Administration Tube Sets are being recalled because supplier changes created a fit issue, so the stopcock cannot be reliably engaged with the Contrast Flow Control Valve.

    Product
    Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2301-2026·2026-06-10

    BD Pyxis Mini Main cabinets may overheat at fingerprint scanner

    BD Pyxis Mini Main medication cabinets are being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn. 709 units affected.

    Product
    BD Pyxis Mini Main REF: 349 Medication cabinet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2262-2026·2026-06-10

    Baxter Exacta Mix inlet sets may contain incorrect 0.8-micron filters

    Exacta Mix Vented Micro-Volume Inlet tubing sets are being recalled because affected lots may contain 0.8-micron filters in place of the validated 3-micron filters.

    Product
    Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0985-2026·2026-06-10

    Albertsons pistachio muffins do not declare walnut allergen

    Albertsons store-made Pistachio Muffins in 2 count and 4 count packs are being recalled because the contains statement does not declare walnut. 354 units are affected.

    Product
    UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 4CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1028-2026·2026-06-10

    Albertsons assorted brownie platter does not declare walnut allergen

    Albertsons store-made Platter Brownies Assorted Seasonal is being recalled because the contains statement does not declare walnut. 15 units are affected.

    Product
    UPC 25511500000 PLATTER BROWNIES ASSORTED SEASONAL This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0986-2026·2026-06-10

    Dubai chocolate parfait cups do not declare pistachio allergen

    Albertsons store-made Parfait Cup Dubai Chocolate is being recalled because the contains statement does not declare pistachio. 25 units are affected.

    Product
    UPC 25606600000 PARFAIT CUP DUBAI CHOCOLATE This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2295-2026·2026-06-10

    Phothera 200 phototherapy calibration certificates had outputs reversed

    Phothera 200 phototherapy devices are being recalled because some Calibration and Output Certificates had the outputs reversed. 368 units are affected.

    Product
    Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2279-2026·2026-06-10

    CASE cardiac testing systems may spark at the printer head

    CASE v7.0 Cardiac Testing Systems are being recalled because electrical sparking may occur at the printer head, and ignition of thermal paper could cause serious thermal injury.

    Product
    CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2026·2026-06-10

    Aligned Medical fluids kits contain recalled lidocaine injection

    Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.

    Product
    Aligned Medical AMS16835 Fluids Kit RX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0568-2026·2026-06-10

    Family Wellness antacid tablets contain small metallic particles

    Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.

    Product
    FAMILY WELLNESS ULTRA STRENGTH ASSORTED FRUIT ANTACID — FAMILY WELLNESS ULTRA STRENGTH ASSORTED FRUIT ANTACID (CALCIUM CARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2284-2026·2026-06-10

    Philips Azurion 3M12 Roadmap Pro may produce unusable dark images

    Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.

    Product
    Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0558-2026·2026-06-10

    Tums assorted fruit antacid tablets contain small metallic particles

    Tums Antacid Assorted Fruit tablets, calcium carbonate 1000 mg in 160-count bottles, are being recalled because of small metallic particles in the chewable tablets.

    Product
    HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC 3 07660 74610 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1074-2026·2026-06-10

    Pavilions chocolate covered strawberries do not declare hazelnut allergen

    Pavilions chocolate covered strawberries, an Albertsons store-made item sold in several counts, are being recalled because the contains statement does not declare hazelnut.

    Product
    UPC 22019700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 1 CT UPC 22117700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 4 CT UPC 22482400000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 10 CT UPC 22126600000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 12 CT
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0968-2026·2026-06-10

    Albertsons gourmet Dubai cookies do not declare pistachio

    Albertsons store-made Gourmet Dubai Cookie is being recalled because the contains statement does not declare pistachio.

    Product
    UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2282-2026·2026-06-10

    Neptune docking station shipped without verified electrical safety testing

    A Neptune Smart Docking Station is being recalled because it was not released from manufacturing and may not have completed required testing, leaving a potential shock risk.

    Product
    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1018-2026·2026-06-10

    Albertsons caesar salads do not declare anchovy allergen

    Albertsons store-made Kitchen Caesar Salads in large and small sizes are being recalled because the contains statement does not declare anchovy. 39 units are affected.

    Product
    UPC 29787600000 Kitchen SALAD CAESAR LARGE SS COLD UPC 21543200000 Kitchen SALAD CAESAR SMALL SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0970-2026·2026-06-10

    Albertsons Mexican wedding cookies do not declare pecan allergen

    Albertsons store-made Mexican Wedding Cookies, 8 count, are being recalled because the contains statement does not declare pecan. 445 units are affected.

    Product
    UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2294-2026·2026-06-10

    Digital angiography and radiography systems may remain energized when switched off

    Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.

    Product
    Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D15
    Category
    Medical Device
    Distribution
    Distributed nationwide