The Recall Desk

Archive

July 2025 recalls

632 recalls were announced in July 2025.

What the numbers show

Critical
4
Severe
232
High
244
Moderate
144
Low
8

Of the 632 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.

601–632 of 632

  • HighFDA (Food)·H-0082-2025·2025-07-02

    Nature Mills Traditional Sambar Powder Recalled for Undeclared Allergens

    NatureMills US Incorporated is recalling Nature Mills Traditional Sambar Powder (200g) due to undeclared sesame and wheat allergens. The product was distributed nationwide via the firm's website.

    Product
    Nature Mills Traditional Sambar Powder, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0080-2025·2025-07-02

    Nature Mills Moringa Leaf Soup recalled for undeclared wheat

    NatureMills US Incorporated is recalling Nature Mills Moringa Leaf Soup (100g) distributed via its website due to undeclared wheat allergens that may pose a risk to consumers with wheat allergies or sensitivities.

    Product
    Nature Mills Moringa Leaf Soup, 100g
    Category
    Food
    Distribution
    0 states
  • HighUSDA FSIS·PHA-07022025-01·2025-07-02

    USDA Issues Public Health Alert for Riverbend Ranch Beef Sticks Due to Plastic

    USDA FSIS issued a public health alert for Riverbend Ranch beef sticks due to possible plastic contamination. No injuries have been reported.

    Product
    Top Notch Jerky LLC — FSIS Issues Public Health Alert for Ready-to-eat Beef Jerky Stick Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1994-2025·2025-07-02

    Barco NexxisOR System Display Encoders and Decoders Recalled

    Barco N.V. is recalling certain NexxisOR system display encoder and decoder models due to duplicate MAC addresses that can cause system malfunction, audio/video interruptions, and delayed procedures when multiple units are deployed together.

    Product
    Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; comp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2024-2025·2025-07-02

    PRIMA 2MM Eccentrical Adaptor With Screw Sterile Medical Device

    Limacorporate is recalling PRIMA 2MM Eccentrical Adaptor With Screw sterile devices because the black laser marking used to identify position may be missing.

    Product
    PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2028-2025·2025-07-02

    REMISOL Advance Medical Device Software Defect Affecting Reference Range Calculations

    A software issue in REMISOL Advance may incorrectly process date-of-birth information from laboratory systems, causing incorrect reference range calculations and potentially auto-validating erroneous test result flags. The actual test results are not changed, but their evaluation may be affected.

    Product
    REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164; C44703; C57017; C69412; C69413; C73942; C73941; C88470; C88471 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 con
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0086-2025·2025-07-02

    Nature Mills Rice Papad recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Nature Mills Rice Papad (200g) because the product contains undeclared wheat allergens. Consumers with wheat allergies should not consume the affected product.

    Product
    Nature Mills Rice Papad, 200g
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·H-0070-2025·2025-07-02

    Big O' Smokehouse Whitefish Spread recalled for plastic contamination

    Big O' Smokehouse is recalling 4lb and 8oz containers of Whitefish Spread due to white plastic fragments found in the product. The affected spread was distributed to retail stores and distributors in Michigan and Illinois.

    Product
    Big O' Smokehouse 4lb Whitefish Spread Big O' Smokehouse 8oz Whitefish Spread Packaged in plastic containers
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1995-2025·2025-07-02

    Medline Umbilical Tray sterile packaging defect recall

    Medline is recalling umbilical trays due to a possible packaging defect in the outer Tyvec pouch that protects the sterile product. The defect may compromise sterility.

    Product
    Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0093-2025·2025-07-02

    Protrim Plus Dietary Supplement Recall for Undeclared Food Dyes

    Protrim Plus dietary supplement 90-capsule bottles contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules. The product was distributed nationwide and may pose a risk to consumers with dye sensitivities or allergies.

    Product
    Protrim Plus, dietary supplement. 90 capsule/bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2033-2025·2025-07-02

    Jewel Precision Sterilization Container System Recalled for FDA Non-Clearance

    Jewel Precision Reusable Rigid Sterilization Container System, Model JP-24-8, was not cleared by the FDA. The letter to file supporting the size change was insufficient.

    Product
    Jewel Precision Reusable Rigid Sterilization Container System. Model Number: JP-24-8.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·H-0088-2025·2025-07-02

    Carley's Soft Baked Iced Lemon Cookies recalled for misbranded color

    Carley's Inc. is recalling Soft Baked Iced Lemon Cookies because the label incorrectly identifies an artificial yellow color instead of listing it as FD&C Yellow #5 as required.

    Product
    Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray, clear film overwrap w/ Label, 12 units per case
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-2012-2025·2025-07-02

    Caphosol Artificial Saliva sachets recalled for out-of-specification stability

    Recordati Rare Diseases is recalling Caphosol Artificial Saliva 32-dose sachets because stability test results for Solution B were out of specification during process validation.

    Product
    Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 mL sachets aqueous solution (32 sachets Solution A Phosphate, 32 sachets Solution B Calcium)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0090-2025·2025-07-02

    Nootri Toto food product recalled due to insanitary conditions

    East Africa Boutique, LLC is recalling Nootri Toto (1 kg packages) distributed to seven retailers in Indiana, Kentucky, Missouri, and Ohio due to products being held under insanitary conditions.

    Product
    Nootri Toto, Net Weight 1 kg, packaged in a cardboard box, packed 12 boxes per case
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1998-2025·2025-07-02

    LUCAS Chest Compression System demonstration units recalled

    Jolife AB is recalling LUCAS 2, 3, and 3.1 chest compression system demonstration units that may have been provided to customers for clinical use instead of demonstration purposes only.

    Product
    LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0089-2025·2025-07-02

    Super Cereal Plus fortified corn soya blend recalled for insanitary conditions

    East Africa Boutique, LLC. is recalling Super Cereal Plus fortified corn soya blend (1.5 kg bags) distributed to retailers in four states because the products were held under insanitary conditions.

    Product
    Super Cereal Plus fortified corn soya blend, Net Weight 1.5 kg, packaged in a plastic foil bag, packed 9 bags per case
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Food)·H-0091-2025·2025-07-02

    Prothin Dietary Supplement Recall for Undeclared Food Dyes

    Preventics, Inc. is recalling Prothin dietary supplement packets because they contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules, which may affect consumers with dye sensitivities or allergies.

    Product
    Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0489-2025·2025-07-02

    Dobutamine Injection Recall Due to Discoloration and Cracked Vials

    Pfizer is recalling one lot of Dobutamine Injection (250 mg/20 mL) nationwide due to discoloration and discolored solution caused by cracked vials. Healthcare facilities should quarantine and return affected units.

    Product
    DOBUTAMINE — DOBUTAMINE (DOBUTAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0094-2025·2025-07-02

    Probese Caps dietary supplement recalled for undeclared food dyes

    Probese Caps, a dietary supplement with Iron sold in 90-count bottles, is being recalled because it contains undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules.

    Product
    Probese Caps, dietary supplement with Iron. 90-count bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0059-2025·2025-07-02

    Madeline's Patisserie Raspberry Croissants Recalled for Undeclared Wheat

    Element 112, LLC is recalling Madeline's Patisserie Raspberry Croissants because they contain undeclared wheat, a major allergen. The recall affects approximately 194 cases distributed to four distributors in Michigan and Ohio.

    Product
    1) Madeline's Patisserie 2.5 ounce Raspberry Croissant, Net Wt. 4 lbs. (1,814.37 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case 2) Madeline's Patisserie 3.5 ounce Raspberry Croissant, Net Wt. 6 lbs. 10 oz. (3,005.05 g), packaged in a
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·H-0092-2025·2025-07-02

    Super ProTHIN Plus Dietary Supplement Recalled for Undeclared Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling Super ProTHIN Plus dietary supplement because gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food colorings.

    Product
    Super ProTHIN Plus, dietary supplement. Seven Packets with 2 tablets & 4 Capsules and 1 packet with 14 Nutrilean capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2027-2025·2025-07-02

    Atellica CH Diluent Contaminated with Sodium Hypochlorite

    Siemens Healthcare Diagnostics is recalling Atellica CH Diluent (SMN 11099300, Lot 0000195412) due to contamination with sodium hypochlorite, which may affect laboratory test results.

    Product
    Product: Atellica CH Diluent - CONS 2 x 1.5L; Siemens Material Number (SMN): 11099300;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2011-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw package labeling mismatch

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because the package labeling lists a different size than the actual product included inside.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 30mm Model/Catalog Number: 506-04-130 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-2026-2025·2025-07-02

    Jewel Precision Reusable Rigid Sterilization Container System Instructions Mismatch

    Jewel Precision Reusable Rigid Sterilization Container System (Model JP-24-6) is being recalled because the Instructions for Use do not match the FDA-cleared indications for use or sterility shelf life.

    Product
    Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0072-2025·2025-07-02

    Nature Mills Sesame Rice Mix recalled for undeclared milk allergen

    NatureMills US Incorporated is recalling Nature Mills Sesame Rice Mix, 200g, due to undeclared milk. The product was distributed in the USA via the firm's website.

    Product
    Nature Mills Sesame Rice Mix, 200g
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0483-2025·2025-07-02

    Tirzepatide Injections Pre-filled Syringe Recalled for Sterility Assurance

    Thrive Health Solutions is recalling Tirzepatide Injections 20mg/mL pre-filled syringes due to lack of assurance of sterility. Approximately 826 syringes distributed nationwide are affected.

    Product
    Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2009-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw labeling mismatch recall

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling lists a different size than the actual product included inside.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 22mm Model/Catalog Number: 506-04-122 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Food)·H-0060-2025·2025-07-02

    Madeline's Patisserie Butter Croissant Buns recalled for undeclared wheat

    Element 112, LLC is recalling Madeline's Patisserie 4.25 Inch Butter Croissant Buns because they contain undeclared wheat, a major food allergen.

    Product
    Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984.47 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case
    Category
    Food
    Distribution
    2 states
  • LowFDA (Food)·H-0062-2025·2025-07-02

    Windsor Brand Extra Coarse Sea Salt Grinder Refill Weight Mismatch

    Windsor brand Extra Coarse Sea Salt Grinder Refill (255 g) does not contain the stated weight of product in each unit. Morton Salt Inc. is recalling 28,820 units distributed in Canada.

    Product
    Windsor brand Extra Course Sea Salt Grinder Refill, 255 g, packaged in a glass jar with plastic lid and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9
    Category
    Food
    Distribution
    0 states
  • LowFDA (Food)·H-0096-2025·2025-07-02

    Rodex Forte dietary supplement recalled for undeclared food dyes

    Rodex Forte dietary supplement (90-capsule bottles) is being recalled because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not listed on the label.

    Product
    Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0095-2025·2025-07-02

    NutriLean Dietary Supplement Contains Undeclared Food Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.

    Product
    NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0061-2025·2025-07-02

    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill recalled

    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill is being recalled because the quantity of product in each unit does not match the stated weight on the packaging.

    Product
    Windsor brand Extra Course Himalayan Pink Salt Grinder Refill, 255 g, packaged in a glass jar with plastic cap and packed 6 units per case, each unit sold individually; Imported by Windsor Salt Ltd., Pointe-Claire, Quebec H9R 5M9
    Category
    Food
    Distribution
    0 states

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