The Recall Desk

State

Montana product recalls

73,509 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total
3,572
Critical
689
Severe
952
Most recent
2026-10-14

Of the 3,572 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 3,572 recalls whose distribution notice names Montana specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25376–25400 of 77081

  • HighFDA (Devices)·Z-1949-2021·2021-06-30

    FDA Recalls Medical Action Minor Procedure Trays for Flaking Metal on Hemostats

    Medical Action Industries is recalling 31 cases of Minor Procedure Trays because hemostats in the kits may have flaking metal or brown spots that could compromise sterile surgical procedures.

    Product
    Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1940-2021·2021-06-30

    OneTouchDelica Lancets Recalled Due to Temperature Exposure During Shipping

    Cardinal Health Inc. is recalling OneTouchDelica Lancets 33G because devices were exposed to freezing temperatures (31.9°F) during shipping, which may cause inaccurate test results.

    Product
    ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0696-2021·2021-06-30

    Clio Strawberry Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Strawberry Greek Yogurt Bars due to the possible presence of metal fragments. The affected product was distributed nationwide.

    Product
    Clio Strawberry Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 861703000113
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1910-2021·2021-06-30

    Ultrasonic Transducer Covers Lack FDA Clearance for Body Cavity Use

    Exact Medical Manufacturing is recalling 7,920 ultrasonic transducer probe covers distributed across six states and Puerto Rico because they lack required FDA 510(k) clearance for use in body cavities and surgical openings.

    Product
    6" x 96" Elastic Poly Probe Cover, T Tip,Tele Fold, 3 bands - Ultrasonic Transducer Cover Item ID: A-AU- 0853NA
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Drugs)·D-0637-2021·2021-06-30

    DermOtic fluocinolone acetonide ear drops recalled for broken glass risk

    Hill Dermaceuticals is recalling DermOtic (fluocinolone acetonide) ear drops due to the potential for broken glass in the glass pipette dropper. The affected product was distributed nationwide.

    Product
    DERMOTIC — DERMOTIC (FLUOCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1920-2021·2021-06-30

    Medical Probe Cover Recalled Due to Missing FDA Premarket Clearance

    Exact Medical Manufacturing recalls 78,000 probe covers that lacked FDA premarket clearance. The product was distributed for use in body openings without required 510(k) approval.

    Product
    Probe Cover, PU and Elastic Blue Bands - 6" x 48", with hole Item ID: SH17
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1923-2021·2021-06-30

    Ultrasound probe covers recalled for missing required FDA 510k clearance

    Exact Medical Manufacturing is recalling 800 units of ultrasound probe covers distributed to six states and Puerto Rico because they lack required FDA 510(k) clearance for use in natural or surgical body openings.

    Product
    Probe Cover, PE, Elastic Bands, 15x244cm-6"x96" -Ultrasonic Transducer Cover Item ID: 1006576
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1929-2021·2021-06-30

    Freestyle Lancets 28G Recalled Due to Temperature Damage During Shipping

    Cardinal Health is recalling Freestyle Lancets due to temperature exposure during shipping that may cause inaccurate results. Affected devices were distributed in Florida, Georgia, and South Carolina.

    Product
    FREESTYLE LANCETS 28G 100CT Item Number:2975670
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0683-2021·2021-06-30

    Clio Berry Acai Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Berry Acai flavored Less Sugar Yogurt Bars in Chocolate Coating due to the possible presence of metal fragments. Affected products have best buy dates between April 11, 2021 and June 27, 2021.

    Product
    Clio Berry Acai flavored Less Sugar Yogurt Bar in a Chocolate Coating 45g x 10 Clio Retail 10-pack, UPC: 854021008244
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V493000·2021-06-30

    2021 Porsche Cayenne steering column screw defect may cause loss of control

    Porsche is recalling 2021 Cayenne vehicles because the screw connecting the steering column to the steering box may fail, potentially detaching the steering column and causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0699-2021·2021-06-30

    Good & Gather Sweet Cajun Trail Mix Recalled for Plastic Pieces

    John B. Sanfilippo & Son Inc. is recalling Good & Gather Sweet Cajun Trail Mix because some packages may contain stringy pieces of flexible plastic.

    Product
    Good & Gather Sweet Cajun Trail Mix, Product Number 04659. with Butter Toffee Peanuts, Spicy Seasoned Peanuts, Cajun Sesame Sticks, Roasted Salted Corn Kernels & Honey Roasted Sesame Sticks. Net Wt 11 oz. (311g), UPC 85239-15700
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1911-2021·2021-06-30

    Ultrasonic Probe Cover Recalled Due to Lack of FDA Clearance for Body Cavity Use

    Exact Medical Manufacturing is recalling 12,650 ultrasonic probe covers (Item A-AU-0980N) that were marketed for use in body cavities without FDA 510(k) clearance.

    Product
    Probe Cover, 6"x96" poly, tapered end, w 3 bands-Ultrasonic Transducer Cover Item ID: A-AU-0980N
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1915-2021·2021-06-30

    Transducer Covers Recalled for Missing FDA 510(k) Clearance

    Exact Medical Manufacturing is recalling 100,600 transducer covers distributed across six states because they lack required FDA 510(k) clearance for use in natural or surgical body openings.

    Product
    Transducer Cover 15x147cm, Kit, VIP Film w/ Bands & EMM Gel Item ID: E6359
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1947-2021·2021-06-30

    novaplus General Purpose Kit hemostats recalled for potential metal flaking

    Medical Action Industries is recalling novaplus General Purpose Kit (Cat. No. 56603) containing hemostats that may have flaking metal and brown spots on the instruments.

    Product
    novaplus, General Purpose Kit, Cat. No. 56603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0700-2021·2021-06-30

    Favorite Day Monster Trail Mix Recalled for Plastic Contamination

    John B. Sanfilippo & Son Inc. is recalling Favorite Day Monster Trail Mix (14 oz, Product Number 04313) because the product may contain stringy pieces of flexible plastic. The recall affects approximately 12,017 cases distributed nationwide.

    Product
    favorite day monster Trail Mix, Product Number 04313. Peanuts, M&M'S Milk Chocolate candies, raisins, milk chocolate chips and Peanut Butter Chips. Net Wt 14 oz. (396g), UPC 85239-15675
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0698-2021·2021-06-30

    Clio Vanilla Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Vanilla Greek Yogurt Bars (50g x 10 pack, UPC 861703000106) due to the possible presence of metal fragments. The recall affects 196,863 cases distributed nationwide with best-by dates between February 14, 2021 and June 27, 2021.

    Product
    Clio Vanilla Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack. UPC code: 861703000106
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1948-2021·2021-06-30

    Surgical instrument trays recalled for potential flaking metal and brown spots

    Medical Action Industries recalls General Purpose Instrument Trays due to potential flaking metal and brown spots on hemostats. These defects could contaminate surgical instruments.

    Product
    Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1921-2021·2021-06-30

    Ultrasonic Transducer Probe Covers Recalled for Missing FDA Clearance

    Exact Medical Manufacturing is recalling 33,250 ultrasonic transducer probe covers lacking required FDA 510(k) clearance for use in natural or surgical body openings, distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.

    Product
    Probe Cover - 6" x 3" x 96"-Ultrasonic Transducer Cover Item ID: SH22
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0689-2021·2021-06-30

    Clio Expresso Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Expresso Greek Yogurt Bars due to the possible presence of metal fragments. The recall affects 6,733 cases distributed nationwide with best-by dates between February 14, 2021 and July 11, 2021.

    Product
    Clio Expresso Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 867155000244
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1908-2021·2021-06-30

    Ultrasonic Transducer Probe Cover Recall: Missing FDA 510(k) Clearance

    Exact Medical Manufacturing is recalling 1,600 ultrasonic probe covers distributed without FDA 510(k) clearance for use in body cavities and surgical openings. Users should discontinue use immediately.

    Product
    Probe Cover 6" x 96" regular PE w/ 3 Elastic Bands- Ultrasonic Transducer Cover Item ID: A-AU-0778NA
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1950-2021·2021-06-30

    Econocare Plus Waffle Overlay Recalled for Bodily Fluid Contamination

    EHOB, Inc. is recalling 70 units of the Econocare Plus Waffle Overlay due to trace amounts of dried bodily fluids that may expose patients and healthcare providers to contaminants.

    Product
    Econocare Plus Waffle Overlay- Intended for use as a medical device to aid in the prevention and treatment of pressure injuries or bed sores and general comfort. Product Code: 1025ECP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1941-2021·2021-06-30

    OptiChamber Diamond Spacer Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling 375 OptiChamber Diamond Spacer devices due to temperature exposure during shipping that may cause inaccurate medication delivery results. Affected devices were distributed to Florida, Georgia, and South Carolina.

    Product
    OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0640-2021·2021-06-30

    Metformin Hydrochloride Tablets Recalled for NDMA Contamination

    Viona Pharmaceuticals is recalling Metformin Hydrochloride Extended-Release Tablets 750 mg due to detection of N-Nitrosodimethylamine (NDMA) levels exceeding acceptable daily intake limits.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1951-2021·2021-06-30

    LEGION Knee Prosthesis Component Recalled for Manufacturing Surface Damage

    Smith & Nephew is recalling 5 units of a knee prosthesis component due to surface damage from a manufacturing error. The affected lot was distributed in specific U.S. states.

    Product
    LEGION Posterior Stabilized OXINIUM Femoral Component, REF 71421216, Size 6, Left, Nonporous Femoral Component, A/P 65.5 MM, M/L 73 MM, For Cemented Use Only, ZR-2.5NB,Sterile. Knee prosthesis component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1916-2021·2021-06-30

    Transducer Cover Lacks FDA 510(k) Clearance for Surgical Use

    Exact Medical Manufacturing is recalling 500 ultrasound transducer covers lacking FDA 510(k) clearance for body cavity use. The affected lot was distributed to Florida, Montana, New York, Ohio, Georgia, and Puerto Rico.

    Product
    Transducer Cover 18x147cm, Kit, VIP Film w/ Bands & EMM Gel- Ultrasonic Transducer Cover Item ID: E6360
    Category
    Medical Device
    Distribution
    6 states