The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

36251–36275 of 50504

  • HighFDA (Drugs)·D-0798-2016·2016-04-06

    Walter's Pharmacy Recalls Tobramycin Ophthalmic Solution Due to Sterility Concerns

    Walter's Pharmacy is recalling Tobramycin 14 mg/mL Ophthalmic Solution because the product lacks assurance of sterility. The recall affects 10 mL bottles distributed in Pennsylvania.

    Product
    Tobramycin 14 mg/mL Ophth Solution, 10mL bottle, Rx only, Walter's Pharmacy, 401 N 17th St, Allentown, PA 610-435-4706, NDC 99999-9996-60
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0811-2016·2016-04-06

    Nestle Trio Low Sodium Brown Gravy Recalled for Metal Fragments

    Nestle USA is recalling Trio Low Sodium Brown Gravy because an ingredient may contain metal fragments.

    Product
    Trio¿ Low Sodium Brown Gravy, 16 ounce, flexible pouch, NET WT 16 OZ CONTAINS: MILK, SOY, WHEAT, INGREDIENTS MAY CONTAIN EGGS DISTRIBUTED BY: NESTLE PROFESSIONAL NORTH AMERICA SOLON, OH 44139
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1006-2016·2016-04-06

    NatureMed Recalls All Day Energy Greens Powdered Drink

    NatureMed Inc. is recalling All Day Energy Greens powdered drink due to reported cases of gastrointestinal distress.

    Product
    All Day Energy Greens Fruity (ADEGF), Great Fruity Taste!, Net Wt 10.5 oz (299g), UPC Code 893320002096 and 893320002423.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1291-2016·2016-04-06

    Ossur Recalls Rebound Air Walkers and Other Medical Devices

    Ossur Americas is recalling Rebound Air Walkers and other medical devices due to a defect described as 'the p'.

    Product
    Rebound Air Walker Product Usage: Rebound Air Walkers are indicated for grade 2 and grade 3 ankle sprains, to stabilize fractures, post-operative use, and trauma or rehab use.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-1295-2016·2016-04-06

    Ossur Recalls Multiple Orthopedic Braces and Medical Devices

    Ossur Americas is recalling various orthopedic braces and medical devices, including the Unloader Custom Lite, due to a defect described in the source text.

    Product
    Unloader Custom Lite Product Usage: Unloader Custom Lite is an external knee braces to provide support for knee instability due to ligament injuries and osteoarthritis.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-1306-2016·2016-04-06

    Siemens CT Systems Recalled for Potential Malfunction Hazard

    Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction hazard when using specific cardio licenses.

    Product
    Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1260-2016·2016-04-06

    ICU Medical Recalls ChemoLock IV Administration Sets Due to Leak Risk

    ICU Medical is recalling specific IV administration sets with ChemoLock ports because the connection may develop a leak.

    Product
    30" (76 cm) Appx. 6.3 ml, 20 Drop Admin Set w/ Integrated ChemoLock Port Drip Chamber, 0.2 Micron Filter, ChemoLock, Hanger, Item No. CL3528 sterile devices intended for the infusion and withdrawal of fluids.
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Food)·F-0998-2016·2016-04-06

    ProSupps Dr. Jekyll Pre-Workout Recalled for Potential Picamilon Content

    ProSupps USA LLC is recalling Dr. Jekyll Intense Pump Pre Workout because it may contain the non-dietary ingredient Picamilon.

    Product
    Prosupps Dr. Jekyll, INTENSE PUMP PRE WORKOUT, 30 SERVINGS, FRUIT PUNCH NATURAL AND ARTIFICIAL FLAVOR DIETARY SUPPLEMENT NET WEIGHT 11.4 OZ (324 GRAMS) packaged in red plastic jars with black lids.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1290-2016·2016-04-06

    Ossur Recalls Multiple Orthopedic Braces and Medical Devices

    Ossur Americas is recalling various orthopedic braces and medical devices, including knee braces and back supports, due to a defect described as 'the p'.

    Product
    Rebound Cartilage Custom Product Usage: Rebound Cartilage Custom is an external knee brace that provides support for knee instability due to ligament injuries and osteoarthritis.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Food)·F-0819-2016·2016-04-06

    Delphi Greek Pepperoncini Recalled for Undeclared Sulfites

    Constantine Poulos and Company is recalling Delphi Greek Pepperoncini due to undeclared sulfites. The product was distributed in five states prior to February 11, 2016.

    Product
    DELPHI GREEK PEPPERONCINI; Peppers, Water, Salt, Vinegar, Citric Acid, Sodium Benzoate. INTERNATIONAL FOODS, INC. BURLINGTON, VT 05401 NET Weight 3 lb. 8 oz. Product is stored at ambient temperature.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1278-2016·2016-04-06

    Siemens Recalls Cios Alpha Mobile X-Ray Systems Due to Software Issues

    Siemens Medical Solutions is recalling 89 Cios Alpha mobile X-ray systems due to software issues. The units were distributed nationwide to 30 states.

    Product
    Cios Alpha, mobile X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2016·2016-04-06

    Siemens Recalls Cios Alpha X-Ray Systems Due to Electrical Shock Risk

    Siemens is recalling four Cios Alpha mobile X-ray systems because a defective part could increase the risk of electrical shock for service personnel during maintenance.

    Product
    CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The Cios Alpha is a mobile X-ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications. Clinical applications may include but are not limited to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1301-2016·2016-04-06

    Siemens CT Systems Recalled for Potential Malfunction Hazard

    Siemens is recalling 124 CT systems due to a potential malfunction hazard when using specific cardio licenses.

    Product
    Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1288-2016·2016-04-06

    Ossur Recalls Multiple Medical Devices Including Miami J Collars

    Ossur Americas is recalling various medical devices, including Miami J collars and knee shields, due to a manufacturing defect.

    Product
    Miami J Collar Product Usage: Miami J collars are applied to patients afflicted with cervical injuries to ensure immobilization.
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-1257-2016·2016-04-06

    ICU Medical Recalls I.V. Infusion Sets with Potential Leak

    ICU Medical is recalling specific I.V. infusion administration sets because a connection may develop a leak. The recall affects 350 units distributed in the US and internationally.

    Product
    110" (279 cm) Appx 13.8 ml, 20 Drop Admin Set w/ Integrated ChemoLock Port Drip Chamber, Clave, Rotating Luer, Bag Hanger, Item No. AHCL3300 sterile devices intended for the infusion and withdrawal of fluids.
    Category
    Medical Device
    Distribution
    14 states
  • HighCPSC·16736·2016-04-05

    Givenchy Recalls Men's Silk T-Shirts for Flammability Violation

    Givenchy is recalling about 60 men's silk T-shirts because they fail to meet federal flammability standards, posing a risk of burn injury.

    Product
    Givenchy men's silk T-shirts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E027000·2016-04-05

    Hale Recalls 6 Inch Suction Strainers Due to Soldering Defect

    Hale Products Inc. is recalling 6 Inch Suction Strainers manufactured between July 2015 and March 2016. Improper soldering may cause the strainer to break, potentially damaging fire pumps and increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V191000·2016-04-05

    Nova Bus Recalls 2010-2015 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2010-2015 LFS transit buses because missing welds on seat J-Brackets may allow seat belt anchorages to separate, increasing injury risk in a crash.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E026000·2016-04-01

    Bosch Recalls Aftermarket Brake Pads for Ford, Lincoln, and Mercury Vehicles

    Bosch is recalling specific aftermarket front brake pads for 1993-2007 Ford, Lincoln, and Mercury vehicles because a shifting shim may damage the brake disc, potentially reducing braking power.

    Product
    FORD — FORD, LINCOLN, MERCURY TAURUS, TAURUS SHO, CONTINENTAL, SABLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V185000·2016-04-01

    Kompact Kamp Recalls Motorcycle Trailers Missing Side Marker Lights

    Kompact Kamp is recalling 1983-2016 Li'l Clipper motorcycle trailers manufactured without side marker lights, which may decrease visibility and increase crash risk.

    Product
    KOMPACT KAMP — KOMPACT KAMP LI'L CLIPPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V186000·2016-04-01

    Pierce Recalls 2010-2016 Vehicles Due to Flashlight Battery Fire Risk

    Pierce Manufacturing is recalling 2010-2016 Arrow-XT, Quantum, and Velocity vehicles because Pelican flashlights may overheat and cause a fire.

    Product
    PIERCE — PIERCE QUANTUM, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide