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.

19926–19950 of 21633

  • ModerateFDA (Food)·F-1932-2013·2013-10-02

    Healthmaxx Global Recalls MAX LIVER STRONG Capsules Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX LIVER STRONG dietary supplements because the label does not match the actual product or ingredients contained.

    Product
    MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Supplement 200 Capsules***6 65176 32608 0***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2283-2013·2013-10-02

    Stryker FL23SE Hospital Bed Recall for Nurse Call Cable Damage Risk

    Stryker is recalling 61 FL23SE adjustable hospital beds because inserting an accessory into the head box slot can damage the nurse call system circuit.

    Product
    The FL23SE Bed is an AC-powered adjustable hospital bed with four built-in electric DC motors and remote controls that is intended for medical purposes. It can be operated by the patient or the caregiver to adjust the height and surface contour of the bed. The bed includes…
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-1926-2013·2013-10-02

    Healthmaxx Recalls Hyper II DHA/EPA Softgels Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling Hyper II DHA/EPA softgels because the label does not match the actual product or ingredients.

    Product
    Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% DHA - 30% EPA***Dietary Supplement 100 Softgels***6 65176 05274 3***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1924-2013·2013-10-02

    Healthmaxx Recalls Brazilian Bee Propolis Softgels Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Brazilian Bee Propolis softgels because the label does not match the actual product or ingredients.

    Product
    MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels***6 65176 31465 0***Manufactured For:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1943-2013·2013-10-02

    Healthmaxx Global Recalls Max Probiotic Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling Max Probiotic-90 tablets because the product label does not match the actual ingredients or product contained.

    Product
    Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Altadena, CA 91001
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F1920-2013·2013-10-02

    Healthmaxx Recalls MAX Kidney Strong Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Kidney Strong tablets because the label does not match the actual product or ingredients.

    Product
    MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:"MAX KIDNEY STRONG***Dietary Supplement 120 Tablets***6 65176 13427 2***Manufactured for: HealthMax Products, Inc. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1922-2013·2013-10-02

    Healthmaxx Global Recalls MAX Brand LIVERAID Dietary Supplement for Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand LIVERAID dietary supplements because the product and ingredient labels do not match the actual contents.

    Product
    MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1912-2013·2013-10-02

    Maplehurst Bakeries Recalls Meijer Carrot Cake Layers Due to Plastic

    Maplehurst Bakeries is recalling Meijer 8-inch carrot cake layers found to contain flexible plastic. The product was distributed in Michigan and Ohio.

    Product
    Meijer 8 Inch Carrot Uniced Split Cake Layers (product is packed in bulk cartons of 24 units/paper bags lined with flexible blue plastic liner).
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-1925-2013·2013-10-02

    Healthmaxx Recalls MAX Bio-Cell Collagen II Softgels for Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Bio-Cell Collagen II softgels because the product label does not match the actual ingredients contained.

    Product
    MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII Dietary Supplement 100 Softgels*** 0 65176 08108 6***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1918-2013·2013-10-02

    Healthmaxx Recalls MAX Brand Glucosamine Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Glucosamine 1500 mg + MSM 400 mg tablets because the label does not match the actual product or ingredients.

    Product
    MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 300 Tablets***6 65176 36159 3***Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA…
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1929-2013·2013-10-02

    Healthmaxx Recalls Stem Cell Enhance Supplements Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Stem Cell Enhance dietary supplements because the product label does not match the actual contents or ingredients.

    Product
    MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2269-2013·2013-10-02

    Smiths Medical Recalls Port-A-Cath Venous Access Systems Due to Sizing Issue

    Smiths Medical is voluntarily recalling Port-A-Cath and Port-A-Cath II implantable venous access systems and introducer sets because the introducer sheath opening may be too small for the catheter.

    Product
    Smiths Medical, Deltec: REF 21-8011-24 Port-A-Cath Dual-Lumen. Titanium Venous Access System. REF 21-8052-24 & REF 21-8053-24 , Port-A-Cath II Dual-Lumen, Polysulfone /Titanium Venous Access System. Sterile EO, Rx Only. PORT-A-CATH¿ and PORT-A-CATH¿ II implantable…
    Category
    Medical Device
    Distribution
    25 states
  • ModerateFDA (Food)·F-1916-2013·2013-10-02

    Healthmaxx Global Recalls MAX Brand Proste-Support Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling 7,074 bottles of MAX Brand Proste-Support tablets because the label does not match the actual product or ingredients.

    Product
    Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads in part:"Manufactured for: HealthMax Products Inc. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1062-2013·2013-10-02

    CorePharma Recalls Pyridostigmine Bromide Tablets Due to Stability Failure

    CorePharma is recalling 960 bottles of Pyridostigmine Bromide Tablets 60 mg because stability testing showed out-of-specification results.

    Product
    Pyridostigmine Bromide Tablets 60 mg, USP Rx Only 100 Tablets, Manufactured and Distributed by: CorePharma, LLC Middlesex, NJ 08846 NDC 64720-128-10 NDC 64720-128-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1914-2013·2013-10-02

    Shenandoah Growers Recalls Fresh Basil Due to Pesticide Adulteration

    Shenandoah Growers is recalling fresh basil that may be adulterated with pesticides. The product was distributed to Pennsylvania, Virginia, and Maryland.

    Product
    Fresh Herbs Everyday Basil, Shenandoah Growers brand, packaged in .75 oz; 2 oz.; and 2.5 oz. in 3 count and 6 count cardboard sleeves and labeled in part ***Shenandoah Growers Inc., Harrisonburg, Va 22802***
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1938-2013·2013-10-02

    Healthmaxx Global Recalls MAX Brand Resveratrol Capsules for Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Resveratrol capsules because the label does not match the actual product or ingredients contained.

    Product
    MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2276-2013·2013-10-02

    Elekta Monaco Radiation Treatment Planning System Software Recall

    Elekta is recalling Monaco RTP System software versions 3.10.00 and later because an upgrade script may overwrite treatment couch files with incorrect default values.

    Product
    Monaco RTP System Radiation treatment planning
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1939-2013·2013-10-02

    Healthmaxx Recalls MAX Brand Soy Isoflavones and Ultra Probiotics for Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Soy Isoflavones and Ultra Probiotics because the labels do not match the actual products or ingredients inside.

    Product
    Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA PROBIOTICS, 90 Count Capsules Product labeling reads in part:"MAX SOY ISOFLAVONES MENOPAUSE SUPPORT**DIETARY SUPPLEMENT 90…
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1915-2013·2013-10-02

    Shenandoah Growers Recalls Fresh Basil Due to Pesticide Adulteration

    Shenandoah Growers is recalling fresh Giant brand basil in 2.5 oz packages because it may be adulterated with pesticides. The product was distributed in PA, VA, and MD.

    Product
    Basil, fresh, Giant brand, packaged in 2.5 oz. package and labeled in part ***Distributed by FoodHold USA Landover, MD 20785***
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1927-2013·2013-10-02

    Healthmaxx Recalls Hyper II Lecithin Softgels Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling 817 bottles of Hyper II Lecithin softgels because the label does not match the actual product or ingredients.

    Product
    Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured for:HealthMax Products Co. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2267-2013·2013-10-02

    Microgenics Recalls DRI Cocaine Metabolite Assay Due to Reagent Degradation

    Microgenics Corp is recalling specific lots of DRI Cocaine Metabolite Assay because surveillance showed unexpected reagent degradation. The recall affects 1,473 units distributed across multiple US states.

    Product
    DRI Cocaine Metabolite Assay, labeled as Multigent Cocaine Assay for Abbott Laboratories. 100 ml, IVD Mfg by: Microgenics Corporation, 46360 Fremont Blvd. Fremont, CA 94538 The DRI Cocaine Metabolite Enzyme Immunoassay is a homogeneous enzyme intended for the…
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Food)·F-1937-2013·2013-10-02

    Healthmaxx Recalls Organic OPC69 Dietary Supplements Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling 3,816 bottles of MAX Brand Organic OPC69 dietary supplements because the label does not match the actual product or ingredients.

    Product
    MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176 51257 3***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2280-2013·2013-10-02

    Horiba Medical Recalls ABX PENTRA Calcium CP Reagent for Incorrect Results

    Horiba Medical is recalling ABX PENTRA Calcium CP Reagent because it may report incorrect calcium results on PENTRA 200 and 400 analyzers.

    Product
    ABX PENTRA Calcium CP Reagent, Model # A11A01633 Calcium plays an essential role in many cell functions: intracellularly in muscle contraction and glycogen metabolism, extracellularly, in bone mineralization, in blood coagulation and in transmission of nerve impulses. Calcium…
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1919-2013·2013-10-02

    Healthmaxx Recalls MAX Glucosamine Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Glucosamine tablets in California, Maryland, and New York because the label does not match the actual product or ingredients.

    Product
    MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg***200 Tablets***6 65176 60566 6***Manufactured in FDA Approved facility for: HealthMax Products, Inc. Altadena, CA 91001***"
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1917-2013·2013-10-02

    Healthmaxx Recalls MAX Glucosamine Tablets Due to Mislabeling

    Healthmaxx Global Inc. is voluntarily recalling MAX Brand Glucosamine tablets because the label does not match the actual product or ingredients.

    Product
    MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 120 Tablets***6 65176 08218 4***Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA…
    Category
    Food
    Distribution
    3 states