The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

2176–2200 of 52931

  • HighFDA (Devices)·Z-1204-2026·2026-02-04

    Evolution Upgrade 1.5T systems recalled over elastography stiffness value errors

    Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2026·2026-02-04

    Feminine hygiene products recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling feminine hygiene products over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2026·2026-02-04

    Q.namix R fluoroscopy systems recalled over unflipped and mismatched images

    Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.

    Product
    Alphenix INFX-8000V, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0422-2026·2026-02-04

    Hamburger dill pickle chips recalled after complaints of glass in product

    Mount Olive Pickle Company is recalling 2,484 cases of Hannaford hamburger dill pickle chips after the firm received complaints of glass found in the product.

    Product
    Hannaford hamburger dill pickle chips 16 FL OZ (1 PT) 473mL glass jar. UPC 0 41268 14889 9 DISTRIBUTED BY: HANNAFORD BROS. CO. SCARBOROUGH, ME 04074
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1167-2026·2026-02-04

    Biocomposite suture anchors recalled after reports of breakage and bending

    Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Fixone Biocomposite Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0436-2026·2026-02-04

    Ginger beer recalled over ginger juice that may be unpasteurized

    Weaver's Brew is recalling 1,070 cases of Goldenroot Lemon Double Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Goldenroot Lemon Double Ginger, Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32819 1. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1208-2026·2026-02-04

    Ingenia 3.0T CX systems recalled over elastography stiffness value errors

    Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    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-1210-2026·2026-02-04

    Ingenia Ambition X systems recalled over elastography stiffness value errors

    Philips North America is recalling 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1215-2026·2026-02-04

    SmartPath dStream 3.0T upgrades recalled over elastography stiffness errors

    Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2026·2026-02-04

    Dual thread screw-in anchors recalled after reports of device failure

    Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V063000·2026-02-04

    Mercedes-Benz Tourrider Buses Recalled for Door Control Valve Defect

    Daimler Coaches is recalling 2026 Mercedes-Benz Tourrider buses because a faulty door valve may prevent doors from opening, delaying emergency evacuation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER PREMIUM, TOURRIDER BUSINESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V064000·2026-02-04

    BMW Recalls 2026 Gran Coupe Models for Rear Light Defects

    BMW is recalling 2026 228i and M235i Gran Coupe vehicles because rear lights may not function properly, increasing crash risk.

    Product
    BMW — BMW M235I XDRIVE GRAN COUPE, 228I XDRIVE GRAN COUPE, 228I GRAN COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1209-2026·2026-02-04

    Ingenia Ambition S systems recalled over elastography stiffness value errors

    Philips North America is recalling 1 unit of the Ingenia Ambition S because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia Ambition S. Product Code (REF): 782108. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1188-2026·2026-02-04

    Bandages and first aid kits recalled over rodent activity in storage

    Gold Star Distribution is recalling first aid kits and bandages over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L; 3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B; 4) PACEMAKER SET UP, Kit SKU DYNJ63377D; 5) PACK PACEMAKER CUSTOM,9909178, Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0420-2026·2026-02-04

    Preserved mustard in soybean oil recalled over undeclared wheat

    New Way Import is recalling 55 cases of Preserved Mustard in Soybean Oil over an undeclared wheat allergen.

    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
    1 state
  • HighFDA (Devices)·Z-1170-2026·2026-02-04

    Lemon ginger hibiscus beer recalled over possibly unpasteurized ginger juice

    Weaver's Brew is recalling 1,014 cases of Goldenroot Lemon Ginger Hibiscus Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Genesis Knotless Anchor
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0421-2026·2026-02-04

    Coconut based strawberry yogurt recalled over undeclared almonds

    Plant Based Innovations is recalling 175 cases of Higher Harvest by H-E-B Dairy Free Coconut Based Strawberry Yogurt Alternative because it contains undeclared almonds.

    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 (Devices)·Z-1203-2026·2026-02-04

    Chest drainage units recalled to limit their use to adults

    Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.

    Product
    Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 4. 8888571370 Cardinal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0439-2026·2026-02-04

    Yuzu ginger lemongrass beer recalled over possibly unpasteurized ginger juice

    Weaver's Brew is recalling 649 cases of Goldenroot Yuzu Ginger Lemongrass Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Goldenroot Yuzu Ginger Lemongrass Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32817 7. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0435-2026·2026-02-04

    Lemon ginger elderberry beer recalled over possibly unpasteurized ginger juice

    Weaver's Brew is recalling 1,066 cases of Goldenroot Lemon Ginger Elderberry Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Goldenroot Lemon Ginger Elderberry Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32818 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0432-2026·2026-02-04

    Green chile and jack cheese tamales recalled over potential Listeria

    Prima Vera Nueva is recalling 31,672 packages (4 tamales per package) of Roasted Green Chile & Jack Cheese Tamales over potential contamination with Listeria monocytogenes.

    Product
    Roasted Green Chile & Jack Cheese Tamales Ingredients: Organic Corn Flour Masa, Roasted Green Chiles, Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt, Enzymes), Non-GMO Corn, Butter, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0430-2026·2026-02-04

    Dairy free butternut squash tamales recalled over potential Listeria contamination

    Prima Vera Nueva is recalling 18,876 packages (4 tamales per package) of Butternut Squash Tamales with Roasted Green Chiles over potential contamination with Listeria monocytogenes.

    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

    Butternut squash tamales recalled over potential Listeria monocytogenes contamination

    Prima Vera Nueva is recalling 30,327 packages (4 tamales per package) of Butternut Squash Tamales With Roasted Green Chiles over potential contamination with Listeria monocytogenes.

    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