The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

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2476–2500 of 30649

  • HighFDA (Food)·H-0430-2026·2026-02-04

    Butternut Squash Tamales Recalled for Potential Listeria Contamination

    Prima Vera Nueva, Inc. is recalling Butternut Squash Tamales with Roasted Green Chiles due to potential contamination with Listeria monocytogenes. The recall affects packages distributed in California and Nevada.

    Product
    Butternut Squash Tamales with Roasted Green Chiles, NO DAIRY Ingredients: Organic Corn Flour Masa, Organic Butternut Squash, Roasted Green Chiles, Non-GMO Corn, Non-hydrogenated Vegetable Shortening, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Cor
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0423-2026·2026-02-04

    Frozen Butternut Squash Tamales Recalled for Potential Listeria Contamination

    Prima Vera Nueva is recalling Butternut Squash Tamales with Roasted Green Chiles due to potential contamination with Listeria monocytogenes. The affected products were distributed in California and Nevada.

    Product
    Butternut Squash Tamales With Roasted Green Chiles, Corn & Jack Cheese Ingredients: Organic Corn Flour Masa, Organic Butternut Squash, Organic Roasted Green Chiles, Non-GMO Corn, Organic Jalapeno Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt and Enzymes), Organic Butter,
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0419-2026·2026-02-04

    McCafe Premium Roast Decaf Coffee K-Cup Pods may contain caffeine despite labeling

    McCafe Premium Roast Decaf Coffee K-Cup Pods are being recalled because they may contain caffeine despite being labeled as decaf. The affected product was distributed in California, Indiana, and Nevada.

    Product
    McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Distributed By: Keurig Green Mountain, Inc. Burlington, MA 01803 U.S.A.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0420-2026·2026-02-04

    Preserved Mustard Recalled for Undeclared Wheat Allergen

    NEW WAY IMPORT INC is recalling Preserved Mustard in Soybean Oil due to undeclared wheat allergen. The product was distributed to 23 retail locations in California.

    Product
    Preserved Mustard in Soybean Oil; original packaging is predominantly green with gold accents and black Chinese lettering. UPC: 6 927393 804265
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0421-2026·2026-02-04

    H-E-B Dairy Free Coconut Yogurt Recalled for Undeclared Almonds

    Plant Based Innovations is recalling 175 cases of HIGHER HARVEST by H-E-B strawberry coconut yogurt because the product contains undeclared almonds, posing a risk to consumers with tree nut allergies.

    Product
    HIGHER HARVEST by H-E-B brand; Dairy Free Coconut Based YOGURT; STRAWBERRY; YOGURT ALTERNATIVE; NET WT 5.3 OZ; INGREDIENTS: COCONUT MILK (WATER, COCONUT CREAM, MODIFIED TAPIOCA STARCH), STRAWBERRIES, CANE SUGAR, WATER, STARCH, NATURAL FLAVOR, FRUITS AND VEGETABLE JUICE (FOR COLOR
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0296-2026·2026-02-04

    Sterile Water for Irrigation Recalled Due to Plastic Particle Contamination

    Baxter Healthcare Corporation is recalling 125,496 units of Sterile Water for Irrigation because plastic particles from the bottle rim have been observed floating into the solution. The nationwide recall affects lot number G171359.

    Product
    STERILE WATER — STERILE WATER (WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1189-2026·2026-02-04

    Medline Medical Procedure Kits Recalled for Defective Tubing

    Medline is recalling three types of medical procedure kits containing MASTISOL liquid adhesive with defective tubing that cracks during use. Approximately 1,928 units were distributed nationwide.

    Product
    Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B; 3) DERMATOLOGY PACK, Kit SKU DYNJT3658A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1191-2026·2026-02-04

    Medline medical procedure kits recalled for defective tubing in adhesive

    Medline Industries recalls 456 surgical procedure kits nationwide due to MASTISOL liquid adhesive with tubing that cracks when actuated. No illnesses have been reported.

    Product
    Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMINAL ENDOSCOPY-LF, Kit SKU DYNJ20027K; 3) LAPAROSCOPY PACK-LF, Kit SKU DYNJ20468J; 4) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763N; 5) SMJ LAPAROSCOPY PACK,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1200-2026·2026-02-04

    Medline medical procedure kits recalled for defective adhesive vial tubing

    Medline Industries recalls 117 surgical procedure kits nationwide due to defective MASTISOL adhesive vials. The tubing in the vials cracks during use, potentially affecting surgical procedures.

    Product
    Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE PACK-LF, Kit SKU DYNJ0395037X; 3) TOTAL HIP PACK, Kit SKU DYNJ04809N; 4) MAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN; 5) SCC/SPOC HAND & FOOT PACK, Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2026·2026-02-04

    Philips MR 7700 MRI Systems May Display Incorrect Elastography Stiffness Values

    Philips MR 7700 MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when MR Elastography images are exported to medical imaging systems, potentially leading to diagnostic errors.

    Product
    MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1166-2026·2026-02-04

    Fixone Hybrid Anchor Medical Device Recalled for Structural Failure Risk

    Aju Pharm Co., Ltd. is recalling Fixone Hybrid Anchor units due to reports of device failure including anchor breakage, bending, and pull-out. All 233 units distributed nationwide in California and Puerto Rico are affected.

    Product
    Fixone Hybrid Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2026·2026-02-04

    Ingenia MR system may display inaccurate elastography stiffness values

    Philips Ingenia 3.0T CX MR imaging systems with software versions R11.1 and R12.1 may display inaccurate tissue stiffness values in PACS viewers, potentially affecting diagnostic accuracy.

    Product
    Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1195-2026·2026-02-04

    Medline procedure convenience kits recalled for defective adhesive vial tubing

    Medline Industries is recalling 1,928 medical procedure kits distributed nationwide. The kits contain MASTISOL liquid adhesive with defective butyrate tubing that cracks during activation.

    Product
    Medline medical procedure convenience kits labeled as: 1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880; 2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1199-2026·2026-02-04

    Medline C-section procedure kits recalled for defective adhesive tubing

    Medline C-section procedure kits are recalled because the MASTISOL liquid adhesive they contain has butyrate tubing that cracks during use.

    Product
    Medline medical procedure convenience kits labeled as: 1) C-SECTION PACK, Kit SKU DYNJ35494C; 2) SMJ C-SECTION PACK-LF, Kit SKU DYNJ38582O; 3) RR-L&D C-SECTION PACK-LF, Kit SKU DYNJ82084F.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0300-2026·2026-02-04

    Glycopyrrolate Oral Solution Recalled for Failed Impurities and Degradation Specifications

    Novadoz Pharmaceuticals is recalling Glycopyrrolate Oral Solution 1 mg/5 mL due to failed impurities and degradation specifications. Patients should contact their healthcare provider about whether to continue medication.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1178-2026·2026-02-04

    Alphenix X-ray System Ceiling Screws May Loosen, Affecting Equipment Movement

    Canon Medical is recalling three Alphenix INFX-8000H interventional x-ray systems. Ceiling-mounted fixing screws may loosen, potentially preventing equipment movement, generating abnormal noise, or triggering sensor errors. No injuries have been reported.

    Product
    Alphenix INFX-8000H, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1184-2026·2026-02-04

    Pregnancy Test 24-Count Recalled Due to Rodent Exposure in Distribution Center

    Gold Star Distribution Inc is recalling Pregnancy Test 24CT units due to potential rodent exposure and rodent activity in the distribution center. The product was distributed in Minnesota.

    Product
    PREGNANCY TEST 24CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1179-2026·2026-02-04

    Alphenix Interventional X-Ray Systems Ceiling Movement Gear Fasteners May Loosen

    Canon Medical's Alphenix INFX-8000V x-ray systems may have loose ceiling movement gear screws, risking loss of ceiling lateral movement, abnormal noise, and sensor errors across 332 units worldwide.

    Product
    Alphenix INFX-8000V, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1180-2026·2026-02-04

    First Aid Kits and Bandages Recalled Due to Rodent Activity

    Gold Star Distribution Inc is recalling First Aid Kit 24/42PC and Lucky First Aid Bandages 24CT due to potential rodent exposure in the distribution center. Products were distributed in Minnesota.

    Product
    Bandages and first aid kits: FIRST AID KIT 24/42PC, LUCKY FIRST AID BANDAGES 24CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1211-2026·2026-02-04

    Philips Ingenia Elition S MR Systems May Display Incorrect Stiffness Values

    Philips recalled five Ingenia Elition S MR systems with software versions R11.1 and R12.1 due to potential stiffness value calculation errors. The issue affects elastography data displayed in PACS viewers worldwide.

    Product
    Ingenia Elition S. Product Code (REF): (1) 781357, (2) 782106, (3)782137. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0298-2026·2026-02-04

    OTC Antacid Tablets Recalled for Failed Disintegration Specification

    Sato Pharmaceutical Co., Ltd. is recalling INON ACE antacid tablets (3,640 bottles, Lot PWXT) distributed in California and Hawaii because the tablets fail to disintegrate according to specification. No illnesses have been reported.

    Product
    INON ACE — INON ACE (MAGNESIUM ALUMINOSILICATES, MAGNESIUM HYDROXIDE, SIMETHICONE)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1202-2026·2026-02-04

    Zimmer A.T.S. 3200TS Tourniquet System may freeze in non-English language settings

    Zimmer Surgical is recalling 51 A.T.S. 3200TS Tourniquet Systems because the device screen may freeze or become unresponsive when operating in non-English language settings. Affected units distributed to Canada and EMEA.

    Product
    Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S.¿ 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Co
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1218-2026·2026-02-04

    LimFlow Vector medical device recalled for incorrect expiration date

    LimFlow Inc. is recalling 33 units of the LimFlow Vector medical device due to incorrect expiration dating on the product label. Healthcare providers should verify the device lot code before use.

    Product
    Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0297-2026·2026-02-04

    Mouthwash Recall: Missing or Illegible Lot and Expiration Date Coding

    Haleon is recalling Parodontax mouthwash due to missing or illegible lot and expiration date coding on bottles. Approximately 84,764 bottles were distributed nationwide.

    Product
    PARODONTAX — PARODONTAX (CETYLPYRIDINIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide