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.

42451–42475 of 50511

  • HighFDA (Food)·F-0199-2014·2013-11-27

    American Beverage Corp Recalls Big Juicy Grape Drink Due to Cap Hazard

    American Beverage Corp is recalling Big Juicy Grape Drink because the sports cap nozzle may dislodge and be ingested. The firm does not anticipate finding impacted product in the market.

    Product
    Big Juicy Grape Drink in 10 oz plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0195-2014·2013-11-27

    American Beverage Recalls Guzzler Alpine Freeze Bottles Due to Cap Hazard

    American Beverage Corp is recalling Guzzler Alpine Freeze bottles because the sports cap nozzle may dislodge if chewed, posing a choking or ingestion risk.

    Product
    Guzzler Alpine Freeze, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0223-2014·2013-11-27

    Sunny Pine Farm Recalls Organic Chevre Due to Pasteurization Concerns

    Sunny Pine Farm is voluntarily recalling Organic Chevre sold in Washington due to possible improper pasteurization.

    Product
    Organic Chevre sold at Farmer's Market in plastic 6 oz tubs, vacuum-sealed with lid and label on top of tub, Sunny Pine Farm brand. Product also sold to in 2 lbs. and 3 lbs. to restaurant. Product is labeled in parts: "***Organic Goat Dairy***Chevre***SUNNY PINE FARM***6…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0364-2014·2013-11-27

    Biomet Recalls Juggerknotless Drill Bits Due to Insertion Difficulty

    Biomet, Inc. is recalling 25 units of Juggerknotless Drill Bits because the design may make it difficult to insert the suture anchor into the bone.

    Product
    Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless Soft Anchors are indicated for soft tissue reattachment procedures in the shoulder, foot/ankle, hand/wrist, and hip.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0197-2014·2013-11-27

    American Beverage Recalls Guzzler Citrus Punch Due to Cap Hazard

    American Beverage Corp is recalling Guzzler Citrus Punch because a part of the nozzle cap may dislodge and be ingested.

    Product
    Guzzler Citrus Punch, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0304-2014·2013-11-27

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Slide Dispense Cartridges

    Ortho-Clinical Diagnostics is recalling Slide Dispense cartridges used with VITROS Chemistry Product Slides due to slide dispense issues.

    Product
    VITROS Chemistry Products CHOL Slides packaged as 300 slides/pack catalog number 1669829 VITROS CHOL Slides quantitatively measure cholesterol (CHOL) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0359-2014·2013-11-27

    Biomet Spine Recalls Polaris Translation Screws Due to Head Dissociation

    Biomet Spine is recalling 7,092 Polaris Translation Screws because the screw head may separate from the shaft. The recall covers nationwide distribution including Puerto Rico.

    Product
    BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0361-2014·2013-11-27

    Aesculap Arcadius XP L Trial Insertion Instrument Recall for Weak Weld

    Aesculap is recalling 30 Arcadius XP L Trial Insertion Instruments because a weak weld may cause the device to disassemble during use.

    Product
    Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0198-2014·2013-11-27

    American Beverage Recalls Big Juicy Blue Raspberry Drink Due to Cap Hazard

    American Beverage Corp is recalling Big Juicy Blue Raspberry Drink bottles due to a potential nozzle cap dislodgement hazard. The firm anticipates finding no impacted product in the market.

    Product
    Big Juicy Blue Raspberry Drink in 10 oz plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0342-2014·2013-11-27

    Trumpf TruSystem Surgical Table Leg Section Recall for Detachment Risk

    Trumpf Medical Systems is recalling 15 TruSystem Surgical Table Leg Section One Part Light components because the coupler point may detach from the frame.

    Product
    TruSystem Surgical Table (TS7000)  Leg Section One Part Light HU Use of the Leg Section One Part Light HU is permitted only with the TRUMPF TruSystem 7000 operating table. The operating table TruSystem 7000, in conjunction with operating table components is intended for the…
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0375-2014·2013-11-27

    Stryker Spine Recalls XIA Torque Wrenches Due to Fracturing Hex Tips

    Stryker Spine is recalling XIA and Mantis Redux torque wrenches because the hex tips may fracture during final tightening.

    Product
    Stryker 1) XIA Torque Wrench 2) XIA 3 Torque Wrench 3) XIA Elegance Short Torque Wrench Manufactured by: Stryker Spine SAS Z.I. Marticot -33610 -CESTAS -FRANCE +33 (0) 5.57.97.06.30 http://www.stryker.com Distributed in the USA by: Stryker Spine 2 Pearl Court…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0182-2014·2013-11-27

    Krispak Recalls Good Sense Spicy Sweet Mix for Undeclared Allergens

    Krispak Inc. is voluntarily recalling one lot of Good Sense Spicy Sweet Mix because it was mislabeled, resulting in undeclared almond and cashew allergens.

    Product
    Good Sense Spicy Sweet Mix, 25-oz (1lb 9oz) plastic container, UPC: 030243787178
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0224-2014·2013-11-27

    Sunny Pine Farm Recalls Organic Parsley Chive Chevre for Pasteurization Concerns

    Sunny Pine Farm is voluntarily recalling Organic Parsley Chive Chevre due to possible improper pasteurization. The product was sold in Washington state.

    Product
    Organic Parsley Chive Chevre sold to non-restaurant in plastic 6 oz plastic tub vacuum-sealed with lid and label on top of tub, Sunny Pine Farm brand. Product sold to restaurant is in 1 lb. and 2 lbs. size. The product is labeled in parts: "***Organic Goat Dairy***Parsley…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0334-2014·2013-11-27

    Zeiss IOLMaster 500 Recalled for Erroneous Lens Database Value

    Carl Zeiss Meditec is recalling 1,201 IOLMaster 500 devices because an incorrect database value for the AMO Sensar AR40E lens could lead to the implantation of lenses with the wrong diopter.

    Product
    Zeiss brand IOLMaster 500, Model 500, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0333-2014·2013-11-27

    Zeiss IOLMaster Recalled for Incorrect Lens Database Value

    Carl Zeiss Meditec is recalling 4,907 IOLMaster devices because an incorrect lens constant in the internal database could lead to the implantation of intraocular lenses with the wrong power.

    Product
    Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0193-2014·2013-11-27

    Guzzler Iced Tea Recalled for Potential Sports Cap Ingestion Hazard

    American Beverage Corp is recalling Guzzler Iced Tea due to a potential risk that a part of the sports cap could be ingested after excessive chewing.

    Product
    Guzzler Iced Tea 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0200-2014·2013-11-27

    American Beverage Corp Recalls Big Juicy Orange Drink Due to Cap Hazard

    American Beverage Corp is recalling Big Juicy Orange Drink in 10 oz plastic bottles because the nozzle cap may dislodge if chewed, posing a health hazard.

    Product
    Big Juicy Orange Drink in 10 oz plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0202-2014·2013-11-27

    American Beverage Corp. Recalls Big Hug Fruit Barrel Grape Bottles

    American Beverage Corp. is recalling Big Hug Fruit Barrel Grape bottles due to a potential choking hazard from dislodged nozzle cap parts.

    Product
    Big Hug Fruit Barrel Grape in a 16 oz plastic bottle with a sports cap, American Beverage Corp., Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0203-2014·2013-11-27

    American Beverage Corp. Recalls Big Hug Fruit Barrel Fruit Punch

    American Beverage Corp. is recalling Big Hug Fruit Barrel Fruit Punch because the sports cap may dislodge and be ingested.

    Product
    Big Hug Fruit Barrel Fruit Punch in a 16 oz plastic bottle with a sports cap, American Beverage Corp., Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0192-2014·2013-11-27

    American Beverage Recalls Guzzler Island Punch Due to Cap Hazard

    American Beverage Corp is recalling Guzzler Island Punch 20 fl. oz. bottles because a part of the nozzle cap may dislodge and be ingested.

    Product
    Guzzler Island Punch 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·14033·2013-11-26

    Burley Recalls Tailwind Bicycle Racks for Trailercycles Due to Fall Hazard

    Burley Design is recalling Tailwind bicycle racks for trailercycles because the top portion can break, causing the trailercycle to disconnect and posing a fall hazard.

    Product
    Tailwind bicycle racks for trailercycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14031·2013-11-26

    American Boy and Girl Recalls Infant Sandals Due to Choking Hazard

    American Boy and Girl is recalling about 1,300 infant girl sandals sold at Meijer stores because the top strap can detach, posing a choking hazard to children.

    Product
    Girl's "Susan" Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V598000·2013-11-25

    Wells Cargo Recalls Trailers Due to Door Lock Jamming Risk

    Wells Cargo is recalling 2006-2013 cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    WELLS CARGO — WELLS CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide