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.

16626–16650 of 21645

  • ModerateFDA (Food)·F-1667-2015·2015-04-08

    Health One Pharmaceuticals Recalls Fish Collagen Dietary Supplements

    Health One Pharmaceuticals is recalling Fish Collagen dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Fish Collagen
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1683-2015·2015-04-08

    Health One Pharmaceuticals Recalls SOD Herbal Mix for cGMP Violations

    Health One Pharmaceuticals is recalling SOD Herbal Mix dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    SOD Herbal Mix
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1672-2015·2015-04-08

    Health One Recalls Gentiana Combination Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling Gentiana Combination dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Gentiana Combination, 100 Vegetarian Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1368-2015·2015-04-08

    Quest Medical Recalls Lacrimal Intubation Sets Due to Labeling Error

    Quest Medical is recalling 106 units of LIS27T Lacrimal Intubation Sets because the expiration date was incorrectly printed in the manufacturing date field.

    Product
    LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1348-2015·2015-04-08

    Microtek Medical Recalls Sterile Laser Resistant Wands Due to Latex Packaging

    Microtek Medical Inc is recalling sterile laser resistant wands because the packaging contains latex but lacks the required warning label.

    Product
    LASER RESISTANT WAND - STERILE, 7/8" X 8" (2.22cm x 20.32cm), REF 24013, QTY 10 EA, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1754-2015·2015-04-08

    Health One Pharmaceuticals Recalls San Ye Qing Dietary Supplements

    Health One Pharmaceuticals is recalling Complex Tablet San Ye Qing dietary supplements due to significant violations of cGMP regulations.

    Product
    Complex Tablet San Ye Qing, 120 tablets, 500mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1668-2015·2015-04-08

    Health One Pharmaceuticals Recalls In Act Xtract Dietary Supplements

    Health One Pharmaceuticals is recalling In Act Xtract dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    In Act Xtract
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1337-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmet Systems Due to Latex Packaging

    Microtek Medical is recalling 10 Freedomaire Surgical Helmet Systems because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET SYSTEM WITH SUPER POWER PAK BATTERY, LUMBAR BELT AND MOTOR MODULE, REF 11110STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1342-2015·2015-04-08

    Microtek Smoke Evacuation Tubing Set Recalled for Latex Packaging Labeling Error

    Microtek Medical Inc is recalling 303 Smoke Evacuation Tubing Sets because the packaging contains latex but lacks the required warning label.

    Product
    Smoke Evacuation Tubing Set for Coherent CPG Handpiece, 7/8" x 16' (2.22 cm x 487.88 cm), REF 24244, QTY 3/CS, NON STERILE NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1773-2015·2015-04-08

    Health One Pharmaceuticals Recalls Vigerect Dietary Supplements

    Health One Pharmaceuticals is recalling Vigerect dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Vigerect
    Category
    Food
    Distribution
    Distributed nationwide