The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

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.

9201–9225 of 21595

  • ModerateFDA (Devices)·Z-1170-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Right, Product No. LJV182T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Food)·F-1301-2019·2019-04-24

    ConAgra Recalls Hunts Tomato Paste Cans Due to Potential Mold

    ConAgra Foods is recalling 145,380 cans of Hunts Tomato Paste No Salt Added due to potential mold caused by can damage.

    Product
    Hunts Tomato Paste No Salt Added 6 ounce cans, 12 per wholesale tray Can UPC: 2700038807 Tray UPC: 2700038809
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1103-2019·2019-04-17

    FDA Recalls Compounded Papaverine-Phentolamine-PGE1 Injectable Due to Insanitary Conditions

    Professional Compounding Pharmacy is recalling compounded Papaverine-Phentolamine-PGE1 injectable due to insanitary conditions observed during a recent FDA inspection.

    Product
    PAPAVERINE-PHENTOLAMINE-PGE1 16.6-0.55 MG-11.1 MCG/ML* INJECTABLE, 10 ml, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330 .
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-1274-2019·2019-04-17

    Impossible Foods Bulk Plant-Based Ground Beef Recalled for Plastic Contamination

    Impossible Foods is recalling 5 lb. bulk plant-based ground beef packs due to a piece of plastic found in the product.

    Product
    Impossible Foods Bulk, 5 lb. vacuum sealed plastic-pack. Keep Frozen; This is a plant product that is looks like and is used like ground beef. UPC: (01) 00816697020036; Item # 60-00010
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-1119-2019·2019-04-17

    Arrow Two-Lumen Central Venous Catheter Set Recalled for Labeling Error

    Arrow International Inc is recalling 45 units of Two-Lumen Central Venous Catheterization Sets due to incorrect priming volume labeling on the lidstock.

    Product
    Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿ Catheter Product Code: CD-10802 GTN: 00801902015396
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Food)·F-1248-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods is recalling 40,250 lbs of Commercial Breader Batter because it may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A81225 BATTER MX X1; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1275-2019·2019-04-17

    Walgreens Probiotic Recalled for Incorrect Bacterial Strain

    Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures because the product contains a different bacterial strain than listed on the label.

    Product
    Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus HN001, L acidophilus La-14, L reuteri L.RE02. Other ingredients: Cellulose, Gelatin, Silicon Dioxide, Magnesium Stearate (vegetable sour
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1251-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods is recalling 2,750 lbs of commercial breader batter that may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A85608 BATTER MX X3; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-1130-2019·2019-04-17

    Lohxa Recalls Bismuth Subsalicylate Suspension Due to Incorrect Expiration Date

    Lohxa LLC is recalling Bismuth Subsalicylate Oral Suspension because the labels contain incorrect expiration dates. The affected product was distributed in Massachusetts, New York, and Wyoming.

    Product
    Bismuth Subsalicylate Oral Suspension 262mg/15mL, unit dose cups, OTC, Rpkg. By.: Lohxa Worcester, MA, NDC 70166-059-01
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1113-2019·2019-04-17

    Gavilyte-N Recalled for Incorrect Flavor Labeling on Orange and Cherry Packets

    Lupin Somerset is recalling Gavilyte-N because orange and cherry flavor packets incorrectly list 'natural lemon flavor' as an ingredient.

    Product
    GAVILYTE-N — GAVILYTE-N (POLYETHYLENE GLYCOL-3350, SODIUM CHLORIDE, POTASSIUM CHLORIDE AND SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1130-2019·2019-04-17

    Philips Recalls Two Azurion FlexArm Units Due to Cable Damage

    Philips is recalling two Azurion FlexArm units because a manufacturing error caused damage to the 24V power cable of the detector.

    Product
    Azurion FlexArm, 722079
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1247-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods Inc is recalling 12,800 lbs of Commercial Breader Batter because it may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A80261 BATTER MX X1; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1111-2019·2019-04-17

    Beaver Xstar Slit Knife Recalled for Size Mismatch Labeling

    Beaver Visitec is recalling 196 boxes of Xstar Slit Knives because the package label indicates a 2.4 mm size, while the device marking shows 2.75 mm.

    Product
    Beaver Xstar Slit Knife 2.4 mm, 45degree Double Bevel, Ophthalmic-utilized in Cataract and Glaucoma procedures REF # 370824 Product Usage: Ophthalmic techniques-utilized in Cataract and Glaucoma procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1262-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods is recalling 20,150 lbs of Commercial Breader Batter because it may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; #22419 BATTER MX X2; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1250-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods Inc is recalling 5,000 lbs of Commercial Breader Batter because it may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A84759 BATTER MX X1; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1255-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods Inc is recalling 32,900 lbs of commercial breader batter that may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A96289 BREADER X1; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Drugs)·D-1131-2019·2019-04-17

    Lohxa Recalls Phenobarbital Oral Solution Due to Incorrect Expiration Date

    Lohxa LLC is recalling Phenobarbital Oral Solution because the labels contain incorrect expiration dates. The affected product was distributed in Massachusetts, New York, and Wyoming.

    Product
    Phenobarbital Oral Solution, USP 20 mg/5mL, unit dose cup, Rx Only, Rpkg. By.Lohxa Worcester, MA 01608 NDC 70166-536-02
    Category
    Drug
    Distribution
    3 states