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.

19526–19550 of 21751

  • ModerateFDA (Devices)·Z-0498-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling certain microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR SL-10 150CM 2 TIP, Catalog Number: M0031681890, Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1106-2014·2013-12-25

    LSG Food World Recalls Noodles House Noodles for Unapproved Additives

    LSG Food World Inc. is recalling Noodles House Home Style Noodles due to the use of an unapproved color and an undeclared food additive.

    Product
    NOODLES HOUSE HOME STYLE NOODLES, Net Wt. 912 g (32 oz), product is packaged in plastic bag with twelve (12) bags per carton. UPC 6 949682 801731. *1st label indicates: Manufactured by: JINYYIFAN(HK)INTERNATIONAL LIMITED RM3.8/F., YUEXIU BLDG., 160-174 LOCKHART ROAD, WAN CHAI…
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0758-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Multi Supplements Due to Chloramphenicol

    National Enzyme Co is recalling bulk digestive supplements that may contain chloramphenicol above 0.3 ppb. The product was distributed domestically and internationally.

    Product
    Bulk 877 HOLISTIC DIGESTIVE MULTI packaged in poly bags within fiber drums (SKU 90461)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0494-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling Excelsior microcatheters because they were shipped with use-by dates exceeding available shelf-life data.

    Product
    Stryker brand EXCELSIOR 1018 PRE-SHAPED 45 150CM, Catalog Number: M0031441900; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0745-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements for Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Houston Enzymes, No-Fenol, Multi-Enzyme Product for Digestion of Phenolic Foods and Fiber packaged in 90-capsule bottles (SKU 52437). Firm name on the label is Houston Nutraceuticals, Inc. (HNI), Siloam, AR…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0530-2014·2013-12-25

    Remel RapID Yeast Plus System Recalled for Mislabeled Reagents

    Remel Inc is recalling 150 kits of the RapID Yeast Plus System because the labels for Reagent A and Reagent B were reversed.

    Product
    remel RapID Yeast Plus System, 20 tests, Ref: R8311007, IVD, containing a 15-ml bottle of RapID Yeast Plus Reagent A and a 10-ml bottle of RapID Yeast Plus Reagent B. Product Usage: For the biochemical identification of medically important yeast and yeast-like organisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0510-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Shelf-Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand COMPLIANT 5MM X 30MM, Catalog Number: M003SRC05300; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-364-2014·2013-12-25

    Tween Brands Recalls Anti-Bac Hand Sanitizer Due to Labeling Error

    Tween Brands Inc is recalling 12,326 bottles of Yum Yum Bubble Gum Justice Anti-Bac hand sanitizer because the label incorrectly states the ethyl alcohol content is 62% instead of 20%.

    Product
    yum yum bubble gum Justice, BUBBLEGUM SCENT ANTI BAC, Ethyl Alcohol, Net Wt. 1 fl oz, Distr by Tween Brands New Albany, OH 43054 Toronto, ON L6T 3R5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0795-2014·2013-12-25

    National Enzyme Recalls Tribulus Supreme 2.0 Supplements Due to Chloramphenicol

    National Enzyme Co is recalling IMTWellnes Tribulus Supreme 2.0 dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    IMTWellnes, Tribulus Supreme 2.0, GI & Immune Support, packaged 60-capsule bottles (SKU 54217). Firm name on the label is ANAT, LLC, Bloomfield, CT;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0790-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplement Formula ID B859; Packaged in the following configuration: B859 Kirkman Enz Comp DPP-IV, packaged in unlabeled, 90-count bottles (SKU 54112);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0502-2014·2013-12-25

    Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates that exceed available shelf-life data.

    Product
    Stryker brand GDC-10 ULTRA SOFT 2MM X 3CM, Catalog Number: M0033432030; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0787-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Bulk B341 Shanghai Actizyme Tab6 tablets, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92275); (2)…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0503-2014·2013-12-25

    Stryker Neurovascular Medical Devices Recalled for Shelf-Life Labeling Errors

    Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.

    Product
    Stryker brand GDC-18 360 18MM X 30CM, Catalog Number: M00334818300; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1113-2014·2013-12-25

    DRUK Orange Squash Recalled for Undeclared Sunset Yellow FCF

    Balajee Trade Link LLC is recalling DRUK Orange Squash because FDA analysis found it contains undeclared sunset yellow FCF.

    Product
    DRUK Orange Squash Contains 25% Orange Juice Net Wt. 24 fl oz. Imported by: Balajee Trade Link, LLC Scranton, PA USA Product of Bhutan
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0736-2014·2013-12-25

    National Enzyme Co Recalls Fiber Digestion Enzyme Supplement Due to Chloramphenicol

    National Enzyme Co is recalling ProSol Professional Solutions Fiber Digestion Enzyme Supplement because it may contain chloramphenicol above the permitted limit.

    Product
    ProSol Professional Solutions Fiber Digestion Enzyme Supplement, packaged in 90-(SKU 51855) capsule bottles. The firm name on the label is Enzymes, Inc., Kansas City, MO
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0835-2014·2013-12-25

    Nature's Way Men's Energizer Tablets Recalled for Potential Antibiotic Contamination

    Schwabe North America is voluntarily recalling Nature's Way Alive Whole Food Energizer Men's tablets because raw material enzymes may contain the antibiotic chloramphenicol.

    Product
    Nature's Way,UPC 33674155424, Alive Whole Food Energizer Men's, 90 Tabs, 20010871
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Food)·F-0774-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Enzyme Powder for Chloramphenicol

    National Enzyme Co is recalling bulk digestive enzyme powder that may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk A123 ORTHOMOLECULAR DIGESTIV powder (SKU 83202), packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0807-2014·2013-12-25

    National Enzyme Recalls Bulk C665 Powder Due to Chloramphenicol

    National Enzyme Co is recalling Bulk C665 powder because it may contain chloramphenicol levels exceeding 0.3 ppb. The product was distributed domestically and internationally.

    Product
    Bulk C665 powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 7256000)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0804-2014·2013-12-25

    National Enzyme Recalls Cellulase Enzymes Due to Chloramphenicol Contamination

    National Enzyme Co is recalling Cellulase Cellulolytic Enzymes because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Cellulase Cellulolytic Enzymes, packaged 100-capsule bottles (SKU 54553). Firm name on the label is Healthy Reflections, Garfield, MN;
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0772-2014·2013-12-25

    National Enzyme Co Recalls Bulk Dietary Supplement Capsules Due to Chloramphenicol

    National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A036 Threshold Ess Enz Ultra capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92131).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0800-2014·2013-12-25

    National Enzyme Co Recalls Bulk Enzyme Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above permitted limits. The product is distributed domestically and internationally.

    Product
    Bulk C434 Shanghai Enzyme Blend B powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83419);
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0837-2014·2013-12-25

    Nature's Way Men's Ultra Potency Tablets Recalled for Chloramphenicol

    Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily Men's Ultra Potency tablets because the raw material supplier reported the enzyme blend may contain the antibiotic chloramphenicol.

    Product
    Nature's Way,UPC 33674156858, Alive Once Daily Men's Ultra Potency, 60 Tabs, 20010553, 20012800
    Category
    Food
    Distribution
    47 states
  • ModerateFDA (Devices)·Z-0544-2014·2013-12-25

    SpineFrontier Recalls PedFuse Reset Pedicle Screws Due to Assembly Error

    SpineFrontier, Inc. is recalling 35 PedFuse Reset pedicle screws because one unit was found assembled with the wrong size screw. The recall covers devices distributed to Virginia and Texas.

    Product
    PedFuse Reset Screw; Model: 01-80115-55 The PedFuse Reset pedicle screw implants intended to be used to help provide immobilization and stabilization of spinal segments as an adjunct to fusion of the thoracic, lumbar, and/or sacral spine.
    Category
    Medical Device
    Distribution
    2 states