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.

37926–37950 of 50506

  • HighFDA (Devices)·Z-2390-2015·2015-08-26

    Sedecal RadPro 40kW Digital X-Ray Panel Recalled for Uncontrolled Movement Risk

    Sedecal S.A. is recalling RadPro 40kW Digital X-Ray systems because electrostatic energy may cause uncontrolled movements that could bump into users or patients.

    Product
    RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray. Intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15226·2015-08-26

    CAMP USA Recalls Tour Nanotech Crampons Due to Fall Hazard

    CAMP USA is recalling Tour Nanotech Automatic and Semi-Automatic crampons because the heel bail can detach, posing a fall hazard. No injuries have been reported.

    Product
    Tour Nanotech Automatic and Semi-Automatic Crampons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2395-2015·2015-08-26

    Winco Drop Arm Care Cliner Chairs Recalled for Fire Hazard

    Winco Mfg. is recalling 30 Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Drop Arm Care Cliner Standard - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2412-2015·2015-08-26

    Teleflex Recalls Tracheopart Sets Due to Connector Detachment

    Teleflex is recalling sterile Tracheopart Sets because the cobb connector may detach from the main connector before use.

    Product
    Tracheopart Set (Left), Sterile
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-2435-2015·2015-08-26

    Siemens Symbia S Series Nuclear Medicine Imaging Systems Recalled for Overheating Risk

    Siemens is recalling Symbia S Series nuclear medicine imaging systems because improper fuses could cause the Power Controller assembly to overheat.

    Product
    Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine (NM) imaging system installed and used in only one location within an imaging facility or in a mobile/ transportable imaging environment.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-2423-2015·2015-08-26

    International Biophysics Recalls IBC Aortic Punch Due to Seal Issues

    International Biophysics Corp. is recalling 10,330 units of IBC Aortic Punch because the heat seal on sterile pouches may not meet strength acceptance criteria.

    Product
    IBC Aortic Punch Catalog Numbers APM40, APL48A, APM44A, APL40A, APM40A, CVAPL36, CVAPL40, CVAPL44, CVAPL48, CVAPL52, APM28BM, APM36BM, APM40BM, APM44BM, APM48BM, APM40BK, APM48BK, APM36BK, APM44BK, APM28, APM36, APL44, APM40 Product Usage: The IBC Aortic Punch is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15225·2015-08-26

    CAMP USA Recalls Blade Runner Crampons Due to Fall Hazard

    CAMP USA is recalling Cassin Blade Runner and Alpine crampons because the front part can break, posing a fall hazard. No injuries have been reported.

    Product
    Cassin Blade Runner and Blade Runner Alpine Crampons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2418-2015·2015-08-26

    Synthes Sciatic Nerve Retractor Recall for Potential Fluid Ingress

    Synthes (USA) Products LLC is recalling 1,113 Sciatic Nerve Retractors due to a potential for micropores to form, which could allow fluid to enter the hollow handle.

    Product
    Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long; Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long are system specific instruments to the 3.5 mm Low Profile Pelvic System Retractor Set.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2975-2015·2015-08-26

    Crystal Farms Shredded Hash Browns Recalled for Golf Ball Slivers

    Michael Foods is recalling Crystal Farms Shredded Hash Browns because the product may contain small slivers of shredded golf ball.

    Product
    Crystal Farms Simply Potatoes Shredded Hash Browns packaged as individual plastic bags Net Wt. 20 oz (1 lb 4 oz) 567 g; UPC 0 20169 22233 4. The 20 oz containers are packed 12 per case (15 lbs total weight); UPC 2 00 20169 22233 8. Distributed by Crystal Farms, Minnetonka, MN.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2405-2015·2015-08-26

    Cordis RenLane Renal Denervation Catheter Recalled for Potential Tip Damage

    Cordis is recalling 98 RenLane Renal Denervation Catheters because the helical tip may be damaged if the arterial access device valve is not fully open.

    Product
    RenLane Renal Denervation Catheter; Cat No.: D135601. Used in adults patients (>18 years) with drug resistant hypertension to denervate the renal arteries to reduce blood pressure.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2401-2015·2015-08-26

    Winco Elite Care Chairs Recalled for Non-Fire Retardant Foam

    Winco Mfg. is recalling 27 Elite Care chairs because the foam used was not fire retardant as required.

    Product
    Winco Elite Care Cliner w/Swing Away Arms X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2429-2015·2015-08-26

    Stryker Recalls Wrist Implants Due to Potential Sterile Barrier Compromise

    Stryker is recalling specific wrist implant models because their sterile packaging may be compromised during transportation.

    Product
    Recon, Radial Implant, Standard Stem, Size 1, Sterile, Do Not Reuse, Rx Only. Intended for replacement of the proximal end of the radius.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2402-2015·2015-08-26

    Winco Inverness Recliners Recalled for Fire Retardant Foam Mislabeling

    Winco Mfg. is recalling 29 Inverness recliners because the foam was mislabeled as fire retardant but is actually standard foam.

    Product
    Winco Inverness 24-Hour Treatment Recliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2963-2015·2015-08-26

    Freedom Snacks Recalls Caramel Popcorn for Undeclared Milk

    Freedom Snacks is recalling 50 bags of Classic Caramel Gourmet Popcorn sold in Washington due to undeclared milk.

    Product
    Classic Caramel Gourmet Popcorn, sold under brand Freedom Snacks, packaged in a flexible plastic bag, net wt. 10 oz.. There is NO UPC. The product is labeled in parts: "***FREEDOM SNACKS***CLASSIC CARAMEL Gourmet Popcorn***Ingredients: popcorn, brown sugar, sugar, corn…
    Category
    Food
    Distribution
    1 state
  • HighCPSC·15222·2015-08-25

    Scag Liberty-Z Lawn Mowers Recalled for Gas Tank Fire Hazard

    Scag Power Equipment is recalling about 4,400 Liberty-Z zero-turn lawn mowers because the gas tank can leak, posing a fire hazard. No injuries have been reported.

    Product
    Scag Liberty-Z zero-turn lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V537000·2015-08-24

    BMW Recalls 2013-2015 G 650 GS Motorcycles for Stalling Risk

    BMW is recalling 1,060 G 650 GS and G 650 GS Sertao motorcycles because they may stall while idling with the clutch pulled in, increasing crash risk.

    Product
    BMW — BMW G 650 GS, G 650 GS SERATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V534000·2015-08-21

    Chrysler Recalls 2014-2015 Ram 1500 Trucks for Side Air Bag Defect

    Chrysler is recalling 2014-2015 Ram 1500 Quad Cab trucks because side air bag curtains may not fully overlap the C-pillars, increasing injury risk in crashes.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E068000·2015-08-21

    Ricon wheelchair lifts recalled due to potential platform failure

    Ricon is recalling specific wheelchair lifts because oversized pivot holes may allow bearings to shift, potentially causing the platform to fall out of the vehicle.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V533000·2015-08-20

    Ford Recalls F-650 and F-750 Trucks for Seat Belt Anchor Defect

    Ford is recalling 2011-2013 and 2015 F-650 and F-750 trucks because passenger seat belt anchors may be installed in the wrong location, increasing injury risk in a crash.

    Product
    FORD — FORD F-650 SD, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2962-2015·2015-08-19

    FITzee Foods Recalls Paleo Turkey Meatloaf Due to Listeria Risk

    Optimal Nutrition is recalling FITzee Foods Paleo Turkey Meatloaf because it contains green beans affected by a Listeria monocytogenes recall.

    Product
    FITzee Foods Paleo Turkey Meatloaf all sizes (small, medium, large and XL)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-2959-2015·2015-08-19

    Restaurant Depot Recalls Frozen Garden Peas Due to Listeria Contamination

    Restaurant Depot is recalling James Farm Garden Peas Chicharos due to Listeria monocytogenes contamination. The product was distributed in Connecticut, Massachusetts, New Jersey, New York, and Pennsylvania.

    Product
    JAMES FARM GARDEN PEAS CHICHAROS, NET Wt. 40 OZ (2.5 LBS), FRESH FROZEN, UPC 7 60695 01000, product is packed in plastic bags and shipped as 12 units/40 oz. per carton, Net Wt. 30lb. Distributed by RD/Jet, LLC 15-24 132 nd Street College Point, NY 11356. PRODUCT OF POLAND.
    Category
    Food
    Distribution
    5 states