The Recall Desk

State

Montana product recalls

73,381 recalls have nationwide distribution and so reach Montana. 3,571 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,571
Critical
689
Severe
952
Most recent
2026-09-23

Of the 3,571 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 952 (27%) are Severe.

These figures cover only the 3,571 recalls whose distribution notice names Montana specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20451–20475 of 76952

  • HighNHTSA·22V541000·2022-07-27

    2022-2023 BMW IX and i4 High-Voltage Battery Fire Risk Recall

    Certain 2022-2023 BMW IX and 2022 i4 vehicles are recalled due to high-voltage batteries that may develop internal damage and short-circuit, posing a fire risk. Owners should not drive or charge the vehicle until the battery is replaced.

    Product
    BMW — BMW IX, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1451-2022·2022-07-27

    Almond Coconut Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Almond Coconut Classic Truffles for undeclared tree nuts (pecans, almonds, coconut, macadamia, walnuts). The affected product was sold in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Almond Coconut Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11025 2. Ingredients: Milk & dark chocolate, honey, butter (pasteurized cream & salt), cream, coconut, almonds, non-fat dry milk, whey, natural flavors, agar, algin & lecithin. Note: Typo on website should be…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1256-2022·2022-07-27

    HYDROmorphone HCl Injection Syringes Recalled for Sterility Assurance

    Nephron Sterile Compounding Center is recalling HYDROmorphone HCl Injection syringes nationwide due to lack of assurance of sterility. The recall affects 12,900 syringes across two manufacturing lots.

    Product
    HYDROmorphone HCl Injection, USP, 6 mg/30 mL (0.2 mg/mL) syringes, 5 x 30 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-529-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1456-2022·2022-07-27

    Chocolate Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Dark on Dark Classic Truffle products due to the potential presence of undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts) that pose an allergen risk to sensitive consumers.

    Product
    Dark on Dark Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 11030 6. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, algin & lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1249-2022·2022-07-27

    Compounded Injectable Medications Recalled for Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 2,315 pre-filled syringes due to lack of sterility assurance. The compounded injectable medication was distributed nationwide.

    Product
    Bupivacaine HCl 150 mg (3.0 mg/mL), Ketorolac Tromethamine 60 mg (1.2 mg/mL), Ketamine HCl 60 mg (1.2 mg/mL) Injection, 50 mL syringes, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1468-2022·2022-07-27

    QBee Sea Salt Caramel Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling QBee Sea Salt Caramel due to undeclared tree nuts. The affected product was sold at ten retail locations in Colorado, New Mexico, and Wyoming, and via internet sales.

    Product
    QBee Sea Salt Caramel. Net wt. 1 oz. PLU Code: 788394 11010 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1434-2022·2022-07-27

    BD Connecta Stopcock recalled for potential housing leakage risk

    Becton Dickinson is recalling BD Connecta Stopcocks due to potential leakage at the housing component. The defect may interrupt treatment and expose patients to biohazardous material.

    Product
    BD Connecta Stopcock Without Extension Tube Catalog No. 394602 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1279-2022·2022-07-27

    Sodium Bicarbonate Injection USP recalled for lack of sterility assurance

    Nephron Sterile Compounding Center recalls 36,354 pre-filled syringes of Sodium Bicarbonate Injection due to lack of sterility assurance. The medication was distributed nationwide.

    Product
    8.4% Sodium Bicarbonate Injection, USP, 4.2 g/50 mL (84 mg/mL) 1 mEq/mL syringe, packaged in 1 x 50 mL Pre-Filled Syringe per carton, 30 x 1 syringe carton per case, Rx Only Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-214-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1411-2022·2022-07-27

    Medical Device Recall: Hill-Rom PRO+ Mattress Microclimate Feature Failure

    Hill-Rom PRO+ mattresses are being recalled for a Microclimate Management feature failure that could increase pressure ulcer risk in patients. The recall affects 200 units distributed in the US and Canada.

    Product
    Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1444-2022·2022-07-27

    Aesculap S4 Cervical Cross Connector Spinal Implant System Recalled for Clamping Failure

    Aesculap Implant Systems is recalling the AESCULAP S4 Cervical Cross Connector (product code SWT113T) used in spinal fusion surgery. The connectors may not clamp properly onto rods, potentially causing movement and wear particles.

    Product
    AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1429-2022·2022-07-27

    Spinal fixation removal key fracture risk under misuse conditions

    The ENNOVATE MIS removal key used in spinal fixation systems may fracture if the 90-degree angle is not maintained during use. A product redesign is underway.

    Product
    ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1402-2022·2022-07-27

    Stryker Triton Canister Scanning Labels Recalled Due to Color Variance

    Stryker is recalling Triton Canister Scanning Labels that may have color variance issues, potentially resulting in lower-than-expected blood loss estimates. The recall affects 16,700 units distributed nationwide.

    Product
    Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label (component part number 11032). A software application used to help estimation of blood loss. Used with blood bearing canisters and accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1281-2022·2022-07-27

    Succinylcholine Chloride Injection Recalled for Sterility Assurance Failure

    Nephron Sterile Compounding Center is recalling 18,840 syringes of Succinylcholine Chloride Injection nationwide because the manufacturing process cannot be assured to have maintained sterility.

    Product
    Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL) syringe, packaged in 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-919-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1436-2022·2022-07-27

    BD Connecta 3-Way Stopcocks Recalled Due to Potential Leakage

    Becton Dickinson recalls BD Connecta 3-Way Stopcocks due to potential leakage at the housing that may delay treatment and expose patients to biohazardous material.

    Product
    BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1267-2022·2022-07-27

    Morphine Sulfate Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling Morphine Sulfate Injection syringes distributed nationwide due to lack of assurance of sterility. Approximately 43,385 syringes are affected.

    Product
    Morphine Sulfate Injection, USP, 2 mg/2 mL (1 mg/mL) syringe, packaged in 5 x 2 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-979-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1454-2022·2022-07-27

    Carmel Classic Truffle Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalled Carmel Classic Truffle candies because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, and walnuts). Consumers with tree nut allergies should not consume this product.

    Product
    Carmel Classic Truffle. Net wt. 1.4 oz. PLU Code: 788394 110005 4. Ingredients: Milk chocolate, honey, ivory chocolate, butter (pasteurized cream & salt), cream, non-fat dry milk, caramel flavor, whey, agar, algin & lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1495-2022·2022-07-27

    Truffle Gift Box Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Truffle Gift Boxes due to undeclared tree nuts that may pose a hazard to allergic consumers. Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Truffle Gift Box PLU Code: 788394 17655 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1252-2022·2022-07-27

    Fentanyl Citrate Injection Recall Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling Fentanyl Citrate Injection nationwide due to lack of assurance of sterility. Approximately 9,410 bags distributed to healthcare facilities are affected.

    Product
    Fentanyl Citrate in 0.9% Sodium Chloride Injection, USP, 2500 mcg/250 mL (10 mcg/mL*) bags, packaged as 10 x 1 IV bag per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-523-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1250-2022·2022-07-27

    Epinephrine Injection Recalled Due to Sterility Assurance Failure

    Nephron is recalling epinephrine injection syringes nationwide due to lack of sterility assurance. No illnesses have been reported to date.

    Product
    EPINEPHrine Injection, USP, 0.1 mg/10 mL (10 mcg/mL) syringes, 5 x 10 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th Street Extension, West Columbia SC 29172, NDC: 69374-544-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1479-2022·2022-07-27

    Honey Caramels Pecan Pearl Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalls Honey Caramels Pecan Pearl due to potential undeclared tree nuts including almonds, coconut, macadamia, and walnuts that may pose a risk to consumers with allergies.

    Product
    Honey Caramels Pecan Pearl. Net wt. 5.87 oz. PLU Code: 788394 12804 2. Ingredients: Honey, butter (pasteurized cream & salt), cream, grade A fancy pecans, nonfat dry milk, whey, pure vanilla, lecithin, algin & agar.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1262-2022·2022-07-27

    Labetalol Injection Recalled Nationwide Over Sterility Assurance Defect

    Nephron Sterile Compounding Center is recalling 184,370 syringes of Labetalol HCl Injection nationwide due to lack of assurance of sterility. Patients using the affected lots should contact their healthcare provider.

    Product
    Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL) syringe, packaged in 5 x 4 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-946-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1248-2022·2022-07-27

    Injectable Lidocaine Syringes Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center has recalled 1,380 prefilled lidocaine syringes nationwide due to inability to confirm product sterility.

    Product
    0.9% Buffered Lidocaine HCl (buffered in 8.4% Sodium Bicarbonate), 45 mg/5 mL (9 mg/mL) syringes, packaged in 5 x 5 mL Prefilled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1278-2022·2022-07-27

    Compounded Sterile Injectable Recalled Due to Lack of Sterility Assurance

    Nephron Sterile Compounding Center LLC is recalling 2210 syringes of a three-drug compounded injectable due to lack of assurance of sterility.

    Product
    Ropivacaine HCl 123 mg (2.46 mg/mL), Clonidine HCl 0.04 mg (0.0008 mg/mL), Ketorolac Tromethamine 15 mg (0.3 mg/mL) Injection, 50 mL syringe, packaged in 5 x 50 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1438-2022·2022-07-27

    BD Connecta White 360 Infusion Connector Recalled for Potential Leakage

    Becton Dickinson recalls BD Connecta White 360 infusion connectors for potential leakage at the stopcock housing. The defect may interrupt treatment and expose patients to biohazardous materials.

    Product
    BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1459-2022·2022-07-27

    German Chocolate Truffle Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling German Chocolate Truffles because they may contain undeclared tree nuts. The recall affects products sold in Colorado, New Mexico, Wyoming, and through nationwide internet sales.

    Product
    German Chocolate Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11058 0.
    Category
    Food
    Distribution
    Distributed nationwide