The Recall Desk

State

Montana product recalls

72,940 recalls have nationwide distribution and so reach Montana. 3,567 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,567
Critical
689
Severe
783
Most recent
2026-09-02

Of the 3,567 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 783 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,567 recalls whose distribution notice names Montana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4701–4725 of 76507

  • CriticalFDA (Food)·H-0150-2026·2025-10-29

    Breakfast burritos and wraps recalled after egg ingredient tested positive for Listeria

    M.C.I. Foods is recalling 1,040 cases of Egg and Cheese Breakfast Burritos and Wraps after the cooked egg ingredient tested positive for Listeria monocytogenes.

    Product
    Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; UPC# 1 070657 477333 9 RTE Egg and Cheese Breakfast Wrap; 2.50 oz; 72 count/case; UPC# 1 070657 497861 1
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0094-2026·2025-10-29

    Basil pesto bowtie salad recalled over recalled pasta ingredient and Listeria

    Kroger is recalling 5,567.4 lbs of Basil Pesto Bowtie Pasta Salad because the store-made deli item contains a pasta ingredient recalled for potential Listeria monocytogenes.

    Product
    Basil Pesto Bowtie Pasta Salad, packaged in plastic containers with various weights, with UPC 217573-1XXXX (sold at deli service counters) or UPC 217573-2XXXX (sold as Grab-n-Go packages in deli departments), under the banners Kroger, Baker's, City Market, Dillons, Fred Meyer, Fr
    Category
    Food
    Distribution
    28 states
  • CriticalFDA (Devices)·Z-0136-2026·2025-10-29

    Impella controllers recalled over purge pressure issues from retainer failures

    Abiomed is recalling Automated Impella Controllers over the potential for purge pressure issues caused by purge retainer failures, covering 9,177 distributed units.

    Product
    Automated Impella Controller (AIC) labeled as the following with corresponding Product Codes: 1. AIC w/Impella Connect for ECP, Product Code: 1000432. 2. Dbl optical, AIC Impella Connect, Phg US, Product Code: 1000201. 3. Impella Controller, Packaged, AU, Product Code: 0042-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0154-2026·2025-10-29

    IV burette sets recalled over missing internal shutoff valve component

    ICU Medical is recalling 23,203 IV administration sets because the burette component is missing an internal shutoff valve intended to stop fluid flow.

    Product
    IV Administration sets. 23" (58 cm) 150 mL Burette Set (Clave, Shut Off) w/Clave, Luer Lock, REF: B33359; 23" (58 cm) 150 ml Burette Set (w/Shut Off), MicroClave, Clamp, REF: B9213; 70" (178 cm) 150 ml Burette Set (Clave, Shut-Off) w/3-Way Stopcock, Clave, Graduated Adapter,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V737000·2025-10-29

    Mazda CX-50 front suspension bolts may allow wheel detachment

    Mazda is recalling certain 2025 CX-50 and CX-50 Hybrid vehicles because the front suspension fastener bolts may not be tightened properly, which can result in suspension component or wheel detachment.

    Product
    MAZDA — MAZDA CX-50, CX-50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0237-2026·2025-10-29

    Blood culture systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 1,086 BD BACTEC Blood Culture Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers: 445570, 445702. 2. INSTRUMENT BACTEC 9120 UNREPAIRED, Catalog Number: 44557008.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0097-2026·2025-10-29

    Opdualag injection vials recalled from one lot over sterility assurance

    Bristol-Myers Squibb is recalling 12,778 vials of Opdualag (nivolumab and relatlimab-rmbw) injection from one lot for lack of assurance of sterility.

    Product
    OPDUALAG — OPDUALAG (NIVOLUMAB AND RELATLIMAB-RMBW)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0207-2026·2025-10-29

    PVC stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Du
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0231-2026·2025-10-29

    ECG trunk cables recalled because improper module placement can cause overheating

    GE is recalling 29,225 MAC VU360 acquisition trunk cables and module holders because incorrect placement of the module can wear the cable until it overheats in use.

    Product
    MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0114-2026·2025-10-29

    Frozen cooked salad shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Arctic Shores branded frozen cooked salad shrimp in 6 oz bags because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores branded Frozen cooked salad shrimp; 6 oz bag UPC: 041130811685
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·H-0113-2026·2025-10-29

    Frozen raw shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen raw shrimp sold under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen Raw shrimp; 2lbs; 1lbs; UPC: 041130810923; 041512179471; 041130810978; 041130811029; 011110641182; 829944010636; 041130811333; 041130810916; 041130812460; 041130810824; 829944012463; 829944012012; 829944004079
    Category
    Food
    Distribution
    34 states
  • HighFDA (Food)·H-0115-2026·2025-10-29

    Tovala frozen raw shrimp recalled over possible cesium 137 contamination

    Southwind Foods is recalling Tovala branded frozen raw phosphate free shrimp in 5 oz bags because it may have been contaminated with Cesium-137.

    Product
    Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0208-2026·2025-10-29

    Silicone stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump silicone dual lumen stomach tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2026·2025-10-29

    Automated microbiology systems recalled after service credentials were accessed by unauthorized actor

    Becton Dickinson is recalling 4,283 BD Phoenix M50 Automated Microbiology Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0210-2026·2025-10-29

    Dual lumen stomach tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of Salem Sump dual lumen stomach tubes with anti-reflux valve after complaints of valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 14 Fr/Ch (4.7 mm) 266130 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve, 16 Fr/Ch (5.3 mm) 266148 Salem Sump" Stomach Tube, Dual Lumen with Anti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0238-2026·2025-10-29

    BD MAX instruments recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 62 BD MAX System instruments after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD MAX System, for in vitro diagnostic (IVD) use, labeled as the following: 1. BD MAX System, BD MAX Instrument, Catalog Numbers: 44191609, 441927.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0216-2026·2025-10-29

    Immunoassay analyzers recalled over dilution factor anomaly affecting patient results

    Beckman Coulter is recalling 571 DxI 9000 Access Immunoassay Analyzers over a software anomaly that may not apply user-specified manual dilution factors, risking false low or high results.

    Product
    DxI 9000 Access Immunoassay Analyzer, Part Number C11137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0235-2026·2025-10-29

    Microbiology data systems recalled after service credentials accessed by unauthorized actor

    Becton Dickinson is recalling 2,050 BD EpiCenter Microbiology Data Management Systems after product service credentials used by some technical support teams were accessed by an unauthorized actor.

    Product
    BD EpiCenter Microbiology Data Management System, labeled as the following: 1. Computer System Epicenter F/G, Catalog Number: 441002. 2. COMPUTER OPTIPLEX EPICENTER SPARE, Catalog Number: 441421. 3. Generic NUC 2, Catalog Number: 445398. 4. Nuc 5i5 Os Image Bow 2.X, C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0232-2026·2025-10-29

    Insulin pumps recalled over software defect causing unexpected correction bolus

    Tandem Diabetes Care is recalling 122,958 t:slim X2 and Mobi insulin pumps because a software defect when paired with a Dexcom G7 sensor may trigger an unexpected automatic correction bolus.

    Product
    t:slim X2 insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014070, 1014071, 1014072, 1014073, and User Guide when using Dexcom G7 sensor; Tandem Mobi insulin pump with Interoperable Technology, Control-IQ+ technology, REF: 1014801, 1014811, 1014813, and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0206-2026·2025-10-29

    ENFit sump tubes recalled after anti-reflux valve breakage complaints

    Cardinal Health is recalling all lots of ENFit Salem Sump PVC tubes after complaints of anti-reflux valve breakage due to excessive force during use.

    Product
    Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E ENFit" SALEM SUMP" PVC TUBE 12FR 48IN 8888264945E ENFit" SALEM SUMP" PVC TUBE 14FR 48IN 8888264960E ENFit" Salem Sump" PVC Tube 16Fr 48IN 8888264986E ENFit" SA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0112-2026·2025-10-29

    Frozen cooked shrimp recalled across four brands over cesium 137 contamination

    Southwind Foods is recalling frozen cooked shrimp under the Arctic Shores, Best Yet, Great American and Master Catch brands because it may have been contaminated with Cesium-137.

    Product
    Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-0233-2026·2025-10-29

    Oral thermometer probes recalled after being programmed with rectal configuration

    Baxter is recalling 5,209 oral probes for Welch Allyn SureTemp Plus thermometers that were inadvertently programmed with the rectal probe configuration and may read low.

    Product
    Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0035-2026·2025-10-29

    Alcohol prep pads recalled from one lot as a subpotent drug

    Medline is recalling 222,800 alcohol prep pads from one lot because the product is subpotent.

    Product
    Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0116-2026·2025-10-29

    Frozen shrimp skewers recalled in expanded cesium 137 contamination action

    Southwind Foods is recalling Great American branded frozen raw shrimp skewers made under insanitary conditions in which the product may have been contaminated with Cesium-137.

    Product
    Great American branded Frozen raw shrimp skewer; 1lb bag UPC: 829944002716; 829944002372
    Category
    Food
    Distribution
    34 states