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.

16701–16725 of 21645

  • ModerateFDA (Food)·F-1764-2015·2015-04-08

    Health One Pharmaceuticals Recalls Super pill#2 Dietary Supplements

    Health One Pharmaceuticals is recalling Super pill#2 dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.

    Product
    Super pill#2
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1708-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cholesterol Formula Due to cGMP Violations

    Health One Pharmaceuticals is recalling Cholesterol Formula capsules due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

    Product
    Cholesterol Formula, 90 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1345-2015·2015-04-08

    Microtek Medical Recalls Sterile Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), WITH TUBING EXTENDER, STERILE, REF 24010, QTY 24\CS, STERILE EO 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-1675-2015·2015-04-08

    Health One Recalls Siberian Ginseng Supplements for cGMP Violations

    Health One Pharmaceuticals is recalling 199 units of Siberian Ginseng supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

    Product
    Siberian Ginseng, 100 capsules, 500 mg
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1339-2015·2015-04-08

    Microtek Medical Recalls Freedomaire Surgical Helmets Due to Latex Packaging

    Microtek Medical Inc is recalling 153 Freedomaire Surgical Helmets because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) HELMET WITH MOTOR MODULE, REF 11113STK, 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 personnel in order to protect against…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1636-2015·2015-04-08

    Health One Pharmaceuticals Recalls Bone Essense Dietary Supplement

    Health One Pharmaceuticals is recalling Bone Essense, 60 capsules, due to significant violations of cGMP regulations for dietary supplements.

    Product
    Bone Essense, 60 capsules
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1749-2015·2015-04-08

    Health One Pharmaceuticals Recalls Protein Powder for cGMP Violations

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

    Product
    Protein Powder
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1767-2015·2015-04-08

    Health One Pharmaceuticals Recalls U O Clear Dietary Supplements

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

    Product
    U O Clear
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1344-2015·2015-04-08

    Microtek Medical Recalls Vacuum Tubing Due to Unlabeled Latex Packaging

    Microtek Medical Inc is recalling non-sterile vacuum tubing because the packaging contains latex but lacks the required warning label.

    Product
    VACUUM TUBING 7/8" X 6' (2.22cm X 182.88cm), REF 24009, QTY 24\CS, NON-STERILE Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include Operating Rooms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1768-2015·2015-04-08

    Health One Pharmaceuticals Recalls Ultra Lecithin Dietary Supplements

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

    Product
    Ultra Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1365-2015·2015-04-08

    Medtronic Recalls Trellis 6 and 8 Peripheral Infusion Systems for Sterility Breach

    Medtronic is voluntarily recalling Trellis 6 and 8 Peripheral Infusion Systems due to potential sterility breaches in the outer packaging.

    Product
    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1706-2015·2015-04-08

    Health One Pharmaceuticals Recalls Cardiospecs Dietary Supplements

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

    Product
    Cardiospecs
    Category
    Food
    Distribution
    Distributed nationwide