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.

701–725 of 3531

  • ModerateFDA (Food)·F-1616-2024·2024-08-14

    Life s a Peach Spritzer Recalled for Unlicensed Facility and Under-Processing

    Urban River Spirits Life s a Peach Spritzer is recalled because it was manufactured in an unlicensed, uninspected facility with potential under-processing. No illnesses have been reported.

    Product
    Life s a Peach Spritzer is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1629-2024·2024-08-14

    Non-Alcoholic Cocktail Mixer Recalled Due to Unlicensed Facility Production

    Urban River Spirits recalls Sunkissed Lavender and Lemon non-alcoholic cocktail mixer (750ml glass bottles) manufactured in an unlicensed, uninspected facility due to potential under-processing concerns.

    Product
    Sunkissed Lavender and Lemon is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0628-2024·2024-08-14

    PEG-3350 Oral Solution Recalled for Defective Non-Sealed Pouches

    A PEG-3350 oral solution is being recalled nationwide due to defective pouches that may not be properly sealed, risking product leakage. The recall affects 13,200 cartons with lot number S300542.

    Product
    PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID — PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID (PEG-3350, SODIUM SULFATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE, SODIUM ASCORBATE AND ASCORBIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1633-2024·2024-08-14

    Non-alcoholic cocktail mixer recalled due to unlicensed production facility

    Urban River Spirits is recalling Raspberry and Peach Melody non-alcoholic cocktail mixer due to concerns over potential under-processing. The product was manufactured in an unlicensed and uninspected facility.

    Product
    Raspberry and Peach Melody is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
    Category
    Food
    Distribution
    0 states
  • ModerateNHTSA·24V852000·2024-08-11

    Air Bag Warning Label Missing on Ford and Lincoln Vehicles

    Ford is recalling certain 2018-2025 Ford and Lincoln vehicles for missing air bag warning labels on the dashboard. The missing label increases risk of crash injury if occupants don't follow proper restraint guidelines.

    Product
    LINCOLN — 2025 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24334·2024-08-08

    SMEG Refrigerators Recalled Due to Detachable Door Injury Hazard

    SMEG USA is recalling about 900 SMEG-branded retro refrigerators because the door can detach and fall off, posing an injury hazard. The firm has received nine reports of doors falling off but no injuries have been reported.

    Product
    SMEG Refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24337·2024-08-08

    Finger-Ease Guitar String Lubricants Recalled Due to Skin Irritation Risk

    Chem-Pak is recalling Finger-Ease Guitar String Lubricants because one production batch contains a contaminant that poses a risk of skin irritation. One report of minor skin irritation has been received.

    Product
    Finger-Ease Guitar String Lubricants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0621-2024·2024-08-07

    Prescription azelaic acid gel recalled for manufacturing process deviations

    Glenmark Pharmaceuticals recalls azelaic acid gel 15% nationwide due to manufacturing process deviations. Patients should consult their healthcare provider about their prescription.

    Product
    AZELAIC ACID — AZELAIC ACID (AZELAIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1517-2024·2024-08-07

    Orzo (Vegan) Dried Recalled Due to Potential Mold Growth

    PASTAURORA LLC is recalling 27 packages of 10oz vegan dried orzo distributed in Washington due to potential mold growth contamination. Consumers should not consume the product.

    Product
    Orzo (vegan) Dried, net wt. 10oz in clear package with green/back printings on white label. UPC 810135110747.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1519-2024·2024-08-07

    NaturesPlus Testosterone Supplement Recalled for Missing Ingredient and Incorrect Formulation

    Natural Organics is recalling NaturesPlus ULTRA T-MALE due to incorrect formulation: the product is missing the ingredient TongKat Ali and contains additional Rhodiola Rosea. No illnesses have been reported.

    Product
    NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost for Men 60 Bi-layer Tablets
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1520-2024·2024-08-07

    NaturesPlus T-MALE Testosterone Support Supplement Recalled for Ingredient Mismatch

    NaturesPlus T-MALE liquid supplement is being recalled because the product is missing the key ingredient TongKat Ali and contains an additional ingredient, Rhodiola Rosea, that should not be present.

    Product
    NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ Berry and 30 OZ Berry
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0623-2024·2024-08-07

    Ciprofloxacin Ophthalmic Solution Recalled Due to Defective Container

    FDC Limited is recalling 66,528 bottles of Ciprofloxacin ophthalmic solution USP 0.3% due to a manufacturing defect in the container cap that prevents access to the medication. All affected bottles were distributed nationwide.

    Product
    CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2453-2024·2024-08-07

    SOFT-VU KUMPE Diagnostic Catheter Recalled for Mislabeled Inner Pouch

    Angiodynamics recalls SOFT-VU KUMPE diagnostic catheters because inner pouch labels may show incorrect catheter length information, while the outer box label is accurate. 519 boxes distributed nationwide.

    Product
    SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2454-2024·2024-08-07

    SOFT-VU KUMPE Catheters Recalled for Mislabeled Inner Pouch

    Angiodynamics is recalling SOFT-VU KUMPE 5F X 65CM angiographic catheters (595 boxes nationwide) because inner pouch labels may show information for a different catheter model while shelf-box labels are correct.

    Product
    SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2439-2024·2024-07-31

    Medical device diagnostic software vulnerability causes potential application crashes

    Siemens Sensis Vibe diagnostic systems may crash when documentation functionality is used during certain reporting events. Seven units were distributed to facilities nationwide.

    Product
    Sensis Vibe systems with software version VD15B in combination with VM VIRTUAL SERVER Model: 10765502-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0614-2024·2024-07-31

    Nature's Script CBD Pain Relief Roll-On Recalled for Subpotent Menthol

    FDA Class III recall of Nature's Script CBD Cryotherapy Pain Relief Roll-on (200mg, 1 oz bottles) due to subpotent menthol content less than the labeled 4%. The product did not contain the claimed amount of active ingredient.

    Product
    Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0616-2024·2024-07-31

    Hemp Bombs CBD Pain Freeze Recalled for Subpotent Menthol Content

    Hemp Bombs CBD Pain Freeze is being recalled because the menthol content is weaker than the labeled 4% claim. The recall affects 2,082 bottles distributed nationwide.

    Product
    Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2422-2024·2024-07-31

    MIC-KEY Gastric-Jejunal Feeding Tube Kits Recalled for Incomplete Safety Information

    Avanos Medical is recalling MIC-KEY Gastric-Jejunal Feeding Tube Kits because the Instructions for Use were missing required risk information about potential complications. No illnesses have been reported.

    Product
    MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 0270xx (Non-ENFIT); and MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Extension Sets with ENFit Connectors, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 8270xx, ste
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0613-2024·2024-07-31

    Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content

    Hemp Bombs CBD Pain Freeze is being recalled because the menthol potency is less than the labeled 4%. Consumers should stop using the affected product and return it to the retailer.

    Product
    Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2425-2024·2024-07-31

    Cystatin C Diagnostic Reagent Marketed Without FDA 510(k) Clearance

    Randox Laboratories is recalling 115 kits of RX Series CYSC Cystatin C Reagent because it was marketed without required FDA 510(k) clearance. Healthcare facilities should discontinue use and contact the manufacturer.

    Product
    RX Series CYSC- Cystatin C Reagent -Intended for in vitro diagnostic (IVD) use as Randox Cystatin C assay on automated analysers. Catalogue Number: CYS4004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1492-2024·2024-07-31

    Dried Plums Recalled for Undeclared Cyclamate Content

    Sweet Preserved Dried Plums from Farmer's Grange contain undeclared cyclamate sweetener. The product was distributed in select U.S. states and should not be consumed.

    Product
    Sweet Preserved Dried Plums; Farmer's Grange; Series Food; 88g; Plastic synthetic (flexible) package; INGREDIENTS: Plum, Salt, Sugar, ADDITIVES: Clove, Cinnamon, Liquorice, Citric acid, Red #40.; Product contains sulfite; PRODUCT OF CHINA (T.F.C).
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0615-2024·2024-07-31

    Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content

    Global Widget LLC is recalling Hemp Bombs CBD Pain Freeze (4% menthol) because the menthol concentration is below the labeled claim. Approximately 11,130 bottles were distributed nationwide.

    Product
    Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateCPSC·24322·2024-07-25

    Essential Values Golf Grip Solvent Recalled for Deceptive Labeling and Poisoning Risk

    Torquay eTrading is recalling Essential Values Golf Grip Solvent and Golf Grip Kits because they are falsely labeled as "Safe and Non-Toxic" and lack required warnings for petroleum distillates, creating a poisoning risk.

    Product
    Essential Values Golf Grip Solvent and Golf Grip Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24314·2024-07-25

    Grand Rapids Chair Company Recalls Wood Dining Chairs Due to Fall Hazard

    Grand Rapids Chair Company is recalling approximately 5,670 wood dining chairs that can shift, break, or collapse, posing a fall hazard. The company has received three reports of the chair breaking, though no injuries have been reported.

    Product
    Wood dining chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1503-2024·2024-07-24

    Emergency Medical Coffee Sweet Cream Canned Beverage Recalled for Potential Under-Processing

    Snapchill, LLC is recalling Emergency Medical Coffee Sweet Cream canned beverages due to potential under-processing. The recall affects 549,146 cans with expiration dates June 16, 2024–April 16, 2025, distributed nationwide in the US and Canada.

    Product
    Coffee + Non-Dairy Creamer + Sugar-Free Sweetener Canned Beverage packaged under the following brands and sizes: 1. Emergency Medical Coffee Sweet Cream, 12 oz. UPC 8 10149-37035 9.
    Category
    Food
    Distribution
    Distributed nationwide