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.

44151–44175 of 50511

  • HighFDA (Devices)·Z-0698-2013·2013-01-30

    Abbott Vitamin D Reagent Kit Recalled for Inaccurate Test Results

    Abbott Laboratories is recalling ARCHITECT 25-OH Vitamin D Reagent Kits because they may produce falsely elevated or depressed results when used with specific Reaction Vessel lots.

    Product
    Abbott Laboratories, ARCHITECT 25-OH Vitamin D Reagent Kit, 03L52-25 (ROW) and 03L52-27 (U.S.) (1 x 100 tests), 03L52-35 (ROW) and 03L52-37 (U.S.) (5 x 100 tests); in vitro diagnostic.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2013·2013-01-30

    ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals

    ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    UltraClean(R) Accessory Electrode 1 inch Coated Needle with Extended Insulation, REF/Catalog No. 139105EXT, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0725-2013·2013-01-30

    ConMed Recalls TUR Endoscopic Cables Due to Compromised Sterile Pouch Seals

    ConMed is recalling 313,190 TUR/Endoscopic Cables because some sterile pouch seals were compromised. No illnesses or injuries have been reported.

    Product
    TUR/Endoscopic Cable, 10 feet (3.05 mm), REF/Catalog No. 135171, Disposable, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13104·2013-01-29

    Columbia Recalls Seven Heated Jacket Models Due to Burn Hazard

    Columbia Sportswear is recalling seven models of heated jackets because the inner wrist cuffs can overheat, posing a burn risk.

    Product
    Men's and Women's Heated Jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V032000·2013-01-29

    Triumph Recalls 2011-2012 Motorcycles Due to Wheel Bearing Quality Issues

    Triumph is recalling specific 2011-2012 motorcycles because wheel bearings of unknown quality could fail, increasing crash risk. Dealers will replace the bearings free of charge.

    Product
    TRIUMPH — TRIUMPH STREET TRIPLE, DAYTONA 675, THUNDERBIRD, THUNDERBIRD STORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V027000·2013-01-25

    PACCAR Recalls 2013 Kenworth and Peterbilt Trucks for Suspension Software Defect

    PACCAR is recalling specific 2013 Kenworth T680 and Peterbilt 567/579 trucks because a software defect may cause the rear air suspension to re-inflate unexpectedly, posing an injury risk.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 567, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V023000·2013-01-24

    GM Recalls Certain 2012 Vehicles for Driver Air Bag Deployment Risk

    General Motors is recalling certain 2012 Chevrolet Camaro, Cruze and Sonic, and Buick Verano vehicles because a driver air bag may fail to deploy in a crash.

    Product
    BUICK — BUICK, CHEVROLET VERANO, CRUZE, SONIC, CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0687-2013·2013-01-23

    Perkinelmer Recalls NEOBASE MSMS Kits Due to Defective Microplate Wells

    Perkinelmer is recalling NEOBASE Non-Derivatized MSMS Kits because the microplate wells used in the assays are defective. This may affect the accuracy of newborn metabolic disorder screening.

    Product
    NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass spectrometry (MSMS) reagent kit is intended for the measurement and evaluation of amino acids, succinylacetone, free carnitine, and acylcarnitine concentrations…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0890-2013·2013-01-23

    Fresh Unlimited Recalls Carrot Coins for Possible Listeria Contamination

    Fresh Unlimited Inc is recalling specific bags of carrot coins due to possible contamination with Listeria monocytogenes. The product was distributed to 15 states.

    Product
    Carrot coin 1/4" 80/2oz bag Item #70263 BEST USED BY 11/21/12 TC: 1 317 2359 15:43
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0898-2013·2013-01-23

    Fresh Unlimited Recalls Shredded Broccoli Fruit Salad Due to Listeria Risk

    Fresh Unlimited Inc is recalling Shredded Broccoli Fruit Salad due to possible contamination with Listeria monocytogenes. The product was distributed to 15 states.

    Product
    SHREDDED BROCCOLI FRUIT SALAD 6.19# (2,807 g) Ingredients: Broccoli, Cauliflower, Apples, Pears, Cole Slaw Dressing***Cranberry***Raisins CONTAINS: Soybean, egg BEST USED BY: 11/23/12 TC: 13171319 15:59***
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0880-2013·2013-01-23

    Unilever Recalls Knorr Pasta Sides for Potential Soy Contamination

    Unilever is recalling Knorr Pasta Sides Cheesy Bacon Macaroni because some pouches may contain soy due to a packaging error.

    Product
    Knorr Pasta Sides Cheesy Bacon Macaroni Net Wt. 3.8 oz, (107 g) Unilever Englewood Cliffs, NJ 07632 USA Made in Canada from domestic and imported ingredients Case SCC 10041000082488 UPC 4100008248
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0893-2013·2013-01-23

    Fresh Unlimited Recalls Diced Red Apples for Listeria Risk

    Fresh Unlimited Inc is recalling diced red apple bags due to possible Listeria monocytogenes contamination. The product was distributed to 15 states.

    Product
    Red Apples DICED 3/4" 5/1# (4,536G) bag Item #71707 Ingredients: Apples (Apples, Calcium Ascorbate), BEST USED BY: 11/25/12 TC: 1 317 2359 15:40 PRODUCT OF: USA
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0674-2013·2013-01-23

    Philips Recalls Brilliance 64 and Ingenuity CT Scanners Due to Software Anomalies

    Philips Medical Systems is recalling nine CT scanning systems due to software anomalies that could pose a risk of injury to patients and personnel if the issues recur.

    Product
    Brilliance 64 and Ingenuity CT Computed Tomography X-Ray Scanning Systems: Brilliance 64 - Model #728231; and Ingenuity CT - Model # 728326, Distributed By: Philips Healthcare, Cleveland, OH. The Brilliance 64 and Ingenuity CT are Computed Tomography X-Ray Systems intended to…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0669-2013·2013-01-23

    Terumo Recalls Sarns High-Flow Aortic Arch Cannulas Due to Connector Flash

    Terumo is recalling Sarns high-flow aortic arch cannulas because connector flash may detach during surgery.

    Product
    Sarns high-flow aortic arch cannula, 5.2 mm (16 Fr) OD with 3/8in connector, 7.5in (19 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0897-2013·2013-01-23

    Fresh Unlimited Recalls Waldorf Salad Kits for Listeria Risk

    Fresh Unlimited Inc is recalling Waldorf Salad Kits due to possible contamination with Listeria monocytogenes. The product was distributed to 15 states.

    Product
    Waldorf Salad Kit 5.19lb (2,345g) bag Item #74802 INGREDIENTS: APPLES***MAYONNAISE***CELERY, WALNUTS CONTAINS: SOYBEAN OIL, EGG, TREE NUTS (WALNUTS) BEST USED BY: 11/23/12 TC: 13171319 15:43
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0670-2013·2013-01-23

    Terumo Recalls Sarns High-Flow Aortic Arch Cannulas Due to Connector Flash

    Terumo is recalling Sarns High-Flow Aortic Arch Cannulas and Flexible Arterial Cannulae because connector flash may detach during surgery.

    Product
    Sarns high-flow aortic arch cannula, 6.5 mm (20 Fr) OD with 3/8in connector, 11in (28 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial Cannulae are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0892-2013·2013-01-23

    Fresh Unlimited Recalls Pineapple Chunks for Possible Listeria Contamination

    Fresh Unlimited Inc is recalling specific bags of Pineapple Chunks due to possible contamination with Listeria monocytogenes. The product was distributed to 15 states.

    Product
    Pineapple Chunks 80/2 oz (4.536g) bag Item #71607, BEST USED BY: 11/21/12 TC: 1 217 2359
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0690-2013·2013-01-23

    Perkinelmer Recalls Defective Truncated V-Bottomed Microplates

    Perkinelmer is recalling specific lots of truncated V-bottomed microplates because the wells are defective. These products are used for preparing and examining human body specimens.

    Product
    Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS Microplate is a general purpose 96 well microplate used in the preparation and examination of specimens from the human body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0667-2013·2013-01-23

    Terumo Recalls Sarns Flexible Arterial Cannulas Due to Connector Flash

    Terumo Cardiovascular Systems is recalling Sarns flexible arterial cannulas and high-flow aortic arch cannulas because the connectors contain flash that may detach during surgery.

    Product
    Sarns flexible arterial cannula, 7.3 mm (22 Fr) OD with 3/8in connector, suture ring, 9.5in (24 cm) long The Sarns" High Flow Aortic Arch Cannula and Sarns" Flexible Arterial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0895-2013·2013-01-23

    Fresh Unlimited Recalls Sliced Radish Bags Due to Listeria Risk

    Fresh Unlimited Inc is recalling specific bags of sliced radishes due to possible contamination with Listeria monocytogenes.

    Product
    Radish Sliced 80/2oz bag Item #74605 BEST USED BY: 11/21/12 TC: 1 317 2359 15:45
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0887-2013·2013-01-23

    Fresh Unlimited Recalls Red Apple Slices for Listeria Risk

    Fresh Unlimited Inc is recalling specific packages of Red Apple Slices due to possible contamination with Listeria monocytogenes.

    Product
    Red Apple Slices 2.4 oz, Item #71746, 20 oz, Item # 71729 14 oz, Item # 71735. Item #71729 is sold under the brand name Sonic UPC 95829 20000. The other two packages are in clear plastic bags.
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-0896-2013·2013-01-23

    Fresh Unlimited Holiday Fruit Delight Kit Recalled for Listeria Risk

    Fresh Unlimited Inc is recalling Holiday Fruit Delight Kits due to possible contamination with Listeria monocytogenes. The product was distributed to 15 states.

    Product
    Holiday Fruit Delight Kit 5.1875 lbs (2,353g) INGREDIENTS: APPLES***RED GRAPES, STRAWBERRY GLAZE***MARSHMELLOW***WALNUTS, ALLERGENS: WALNUTS (TREE NUTS) BEST USED BY 11/23/12 TC: 13171319 15:42
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-0695-2013·2013-01-23

    Stryker Recalls Hoffman LRF Wire Bolts Due to Breakage During Use

    Stryker Howmedica Osteonics is recalling 476 Hoffman LRF Wire Bolts because two complaints reported the wires broke during load-bearing application by patients.

    Product
    Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
    Category
    Medical Device
    Distribution
    Distributed nationwide