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.

17651–17675 of 21645

  • ModerateFDA (Food)·F-0300-2015·2014-11-05

    Good Herbs HMC Recalled for Failure to Meet GMP Standards

    Good Herbs, Inc. is recalling HMC 4 oz bottles because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., HMC, 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0361-2015·2014-11-05

    Good Herbs Oatstraw Recalled for Failure to Meet GMP Standards

    Good Herbs, Inc. is recalling Oatstraw herb bottles because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., OATSTRAW, 1 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0206-2015·2014-11-05

    Good Herbs Aspen Flower Essence Recalled for GMP Violations

    Good Herbs, Inc. is recalling Aspen Flower Essence bottles because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., FLOWER ESSENCE ASPEN, 1 & 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0178-2015·2014-11-05

    Good Herbs Dong Quai Recalled for GMP Violations

    Good Herbs, Inc. is recalling Dong Quai bottles because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., DONG QUAI, 1 & 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0332-2015·2014-11-05

    Good Herbs Lung Support 1 Recalled for GMP Violations

    Good Herbs, Inc. is recalling Lung Support 1 herbal supplements because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., LUNG SUPPORT 1, 1 & 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0196-2015·2014-11-05

    Good Herbs Eyebright Recalled for Failure to Meet GMP Standards

    Good Herbs, Inc. is recalling Eyebright products because they were not manufactured under Good Manufacturing Practices (GMPs).

    Product
    Good Herbs, Inc., EYEBRIGHT, 1 & 4 oz bottle, 550 Oliver Dr Troy, MI 48084 The Quality Herb That Works
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Food)·F-0052-2015·2014-10-29

    Logan's Roadhouse Meatloaf Mix Recalled for Egg Spoilage Risk

    Processed Foods, Inc. is recalling 380 units of Logan's Roadhouse Meatloaf Mix because the eggs used in the product are susceptible to premature spoilage.

    Product
    Logan's Roadhouse Meatloaf Mix #25018, Keep Frozen, Net Weight: 40 Lbs. (20 - 2 Lb. Bags), FOR INSTITUTIONAL USE ONLY, Custom Foods of America, Knoxville, TN 37921
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Food)·F-0053-2015·2014-10-29

    Perkins Meatloaf Mix Recalled Due to Egg Spoilage Risk

    Processed Foods, Inc. is recalling Perkins Meatloaf Mix because it contains eggs susceptible to premature spoilage.

    Product
    PERKINS Meatloaf Mix #31607, Keep Frozen, Net Weight: 20.125 Lbs. (7 - 2.875 Lb. Bags), FOR INSTITUTIONAL USE ONLY, Custom Foods of America, Knoxville, TN 37921
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0121-2015·2014-10-29

    Aerogen Nebulizer Power Adapter Recall Due to Broken Cover

    Aerogen is recalling 323 FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover broke and dislodged from the adapter body.

    Product
    The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0061-2015·2014-10-29

    Michael Foods Recalls Papetti's Pre-cooked Scrambled Eggs Due to Spoilage Risk

    Michael Foods is recalling Papetti's Table Ready Refrigerated pre-cooked scrambled eggs because the product may be contaminated with a spoilage microorganism.

    Product
    Papetti's Table Ready Refrigerated pre-cooked scrambled eggs. Keep refrigerated 33 - 40 degrees F. Packaged in two different size configurations: (1) 12- 1.85 pound bags, Net Wt. 22.2 lbs (10.06 kg). Product code: 46025-85878. UPC Code: 1 07 46025 85878 9, and (2) 8…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0060-2015·2014-10-29

    Michael Foods Recalls Papetti's Scrambled Eggs for Microbial Contamination

    Michael Foods is recalling Papetti's Table Ready scrambled eggs due to potential contamination with a spoilage microorganism. The product was distributed nationwide.

    Product
    Papetti's Table Ready Refrigerated pre-cooked scrambled eggs with butter flavor. Keep refrigerated 33 - 40 degrees F. Packaged in 12- 1.85 pound bags with Net Wt. 22.2 lbs (10.06 kg). Product code: 46025-85877. UPC Code: 1 07 46025 85877 2.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D0035-2015·2014-10-29

    New Gpc Inc. Recalls Rector's Remedy Ointment for Labeling Deficiencies

    New Gpc Inc. is recalling Rector's Remedy Ointment because the product lacks required drug listings and OTC labeling.

    Product
    Rector's Remedy OINTMENT, Net Contents: 15g. Manufactured by: NEW GPC INC. A1 Farm, EBD. Country of Origin Guyana.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0120-2015·2014-10-29

    Aerogen Nebulizer Power Adapter Recall Due to Broken Cover

    Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.

    Product
    The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0051-2015·2014-10-29

    Golden Corral Meatloaf Mix Recalled for Egg Spoilage Risk

    Processed Foods, Inc. is recalling Golden Corral Meatloaf Mix because it contains eggs susceptible to premature spoilage.

    Product
    Golden Corral MEATLOAF MIX #18029, KEEP FROZEN, NET WEIGHT: 20 lbs (4 - 5 lb Bags), FOR INSTITUTIONAL USE ONLY, Manufactured Exclusively for GC Corporation, Raleigh, NC 27612
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0117-2015·2014-10-29

    Straumann Dental Implant Recall Due to Incorrect Component Assembly

    Straumann USA is recalling 6 units of Bone Level Tapered Dental Implants because they were assembled with the wrong transfer piece.

    Product
    Straumann Bone Level Tapered Implant 04.1 mm RC, SLActive¿ 8mm, Roxolid¿, Loxim Article Number: 021 .5308 Dental implants are intended for surgical placement in maxillary and/or mandibular arches to provide support for prosthetic restorations in edentulous or partially…
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0109-2015·2014-10-29

    Signal Medical Recalls Microseal Hip Liners Due to Incorrect Dimensions

    Signal Medical Corporation is recalling 12 Microseal Augmented acetabular liners because four units were found to have incorrect dimensions.

    Product
    Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM F648). Sizes 36x52x20; and 36x50x20. Device is intended for use with Whiteside Biomechanics, Inc./Signal Medical Corporation Micro-Seal Shell in an uncemented Total Hip…
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0111-2015·2014-10-29

    Signal Medical Recalls Total Knee Femoral Components Due to Packaging Compromise

    Signal Medical Corporation is recalling 41 Symmetric Total Knee Femoral Components because their packaging was compromised. The components were distributed in Missouri and Panama.

    Product
    Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee Femoral Component is intended for use with Signal Medical Corp. Total Knee System for cemented use INA Total Knee Replacement. The femoral component is made of cobalt chromium alloy (ASTM F75).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0093-2015·2014-10-29

    McKesson Cardiology Hemo Software Recall Due to Insufficient Maintenance Communication

    McKesson Information Solutions LLC is recalling 625 McKesson Cardiology Hemo devices because communication regarding required annual maintenance testing was insufficient.

    Product
    McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D0033-2015·2014-10-29

    New GPC Inc. Recalls Whitfield Lotion for Labeling Deficiencies

    New GPC Inc. is recalling 360 units of Whitfield Lotion in New York because the product lacks required OTC drug listing and labeling.

    Product
    WHITFIELD LOTION, Net Contents: 60 mL. Manufactured by: NEW GPC INC. A1 Farm, EBD. Country of Origin Guyana.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D0032-2015·2014-10-29

    New GPC Inc. Recalls Ferrol Expectorant for Labeling Deficiencies

    New GPC Inc. is recalling Ferrol Expectorant because the product lacks required OTC drug listings and labeling, and is labeled as not approved for sale in the U.S.

    Product
    Ferrol EXPECTORANT, Net Contents: 100 mL. Product packaged within a plastic bottle individually placed in small blue carton. Manufactured by: NEW GPC INC. A1 Farm, EBD. Country of Origin Guyana.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0028-2015·2014-10-29

    Bio-Pharm Recalls Acetaminophen Oral Suspension Due to Assay Failure

    Bio-Pharm, Inc. is recalling one lot of Acetaminophen Oral Suspension Liquid 160mg/5mL because the product failed the assay at the 6-month timepoint.

    Product
    Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL, Cherry Flavor, 2 FL. oz bottle, OTC, Distributed by: Rugby Laboratories Livonia, MI 48150, NDC 0536-3606-96 Major Children's Mapap Suspension Liquid, Cherry Flavor, 4 FL OZ bottle, OTC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0107-2015·2014-10-29

    Mindray V-Series Patient Monitor Recalled for Drug Calculator Function Issue

    Mindray DS USA is voluntarily recalling V-Series Patient Monitors due to a software issue with the Drug Calculator function.

    Product
    Mindray V21, Size: 515 mm X 335 mm X 685 mm, N.W.: 8 kg, G.W.: 11 kg, Qty:1 The V-Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for use include the monitoring of ECG waveform derived from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0036-2015·2014-10-29

    Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failure

    Forest Pharmaceuticals is recalling Bystolic (nebivolol) 20 mg tablets because they failed a dissolution specification at a 6-month stability time point.

    Product
    Bystolic (nebivolol) tablets, 20 mg/tablet, packaged as 7 tablets/bottle/carton, and 12 bottles/trays, Professional Sample, Rx only, Forest Pharmaceuticals, Inc., St. Louis, MO. --- NDC 0456-1420-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D0029-2015·2014-10-29

    New GPC Inc. Recalls Alcosulph Moisturizing Cream for Labeling Deficiencies

    New GPC Inc. is recalling Alcosulph Moisturizing Cream because it lacks required OTC drug listings and labeling, and is marked not approved for sale in the U.S.

    Product
    alcosulph Moisturizing Cream, Net Contents: 60g. Product packaged within a plastic container individually placed in small carton. Country of Origin Guyana.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Food)·F-0054-2015·2014-10-29

    Flying Biscuit Oatmeal Pancake Batter Recalled for Egg Spoilage Risk

    Processed Foods, Inc. is recalling Flying Biscuit Oatmeal Pancake Batter because the eggs used in the product are susceptible to premature spoilage.

    Product
    FLYING BISCUIT, Oatmeal Pancake Batter #70002, Keep Frozen, Net Weight: 20 Lbs. (4 - 5 Lb. Bags), FOR INSTITUTIONAL USE ONLY, Custom Foods of America, Knoxville, TN 37921
    Category
    Food
    Distribution
    9 states