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.

23401–23425 of 50435

  • HighFDA (Devices)·Z-1618-2020·2020-04-08

    Karl Storz C-MAC Video Laryngoscope Recall Due to Loose Glass Cover

    Karl Storz is recalling 27,165 C-MAC Video Laryngoscopes because the glass cover at the distal end may become loose during use or reprocessing, potentially delaying procedures or requiring removal from the body.

    Product
    Karl Storz SE & Co. KG, C-MAC Video Laryngoscope MIL # 1, for the following REF numbers: 1. 8403xx series, which includes: 8403AX, AXC, BX, BXC, DXC, EXC, GXC, HX, HXK, HXP, KXC, MXC 2. 8401xx series, which includes: 8401AX, AXC, BX, BXC, DXC, GXC, HX, HXP, KXC.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1620-2020·2020-04-08

    Stryker AXS Vecta 71 Aspiration Catheter Recall for Breakage Risk

    Stryker Neurovascular is recalling AXS Vecta 71 Aspiration Catheters because they may break, fracture, or kink if improperly removed or during use.

    Product
    Stryker Neurovascular, AXS Vecta 71 Aspiration Catheter, Ref. Catalog No. INC-11129-115, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Bayside Parkway, Fremont, CA 94538, UDI: (01)07613327459210(17)211129(10)00000-00 Stryker…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0875-2020·2020-04-08

    Advanced Fresh Concepts Recalls Cooked Butterfly Shrimp Due to Vibrio

    Advanced Fresh Concepts Corp is recalling cooked butterfly shrimp after firm testing detected Vibrio parahaemolyticus. The product was distributed in 38 states.

    Product
    Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC Distribution Corp. Rancho Dominguez, CA
    Category
    Food
    Distribution
    40 states
  • HighFDA (Devices)·Z-1621-2020·2020-04-08

    Stryker AXS Vecta 74 Aspiration Catheter Recall for Potential Fracture

    Stryker Neurovascular is recalling 1,405 AXS Vecta 74 Aspiration Catheters because they may break, fracture, or kink if improperly removed or during use.

    Product
    Stryker Neurovascular, AXS Vecta 74 Aspiration Catheter, Ref. Catalog No. INC-11597-115, Use By 2021-11-29, Rx Only, Sterile/EO, Manufactured For: Stryker Neurovascular 47900 Bayside Parkway, Fremont, CA 94538, UDI: (01)07613327459241(17)211129(10)00000-00 Stryker…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1603-2020·2020-04-08

    Maquet Recalls Avalon Elite Vascular Access Kits Due to Needle Mix-up

    Maquet is recalling 255 Avalon Elite Vascular Access Kits because 81 units were assembled with an incorrect arterial needle instead of a multi-purpose needle.

    Product
    Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·F-0870-2020·2020-04-08

    McClancy Dirty Rice Mix Recalled for Blue Plastic Slivers

    McClancy Seasoning Company is recalling Bojangles Complete Dirty Rice Mix because it contains blue plastic slivers. The product was distributed to Florida, Georgia, and North Carolina.

    Product
    Case Label: Rice Dirty Mix Comp 24-17.9 oz bags/case, PACKED EXCLUSIVELY FOR: BR 9432 SOUTHERN PINE BLVD. CHARLOTTE, NC 28273. Bag Label: Bojangles Complete Dirty Rice Mix Net Wt: 17.9 oz bags
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0876-2020·2020-04-08

    Vitamin Cottage Peanut Clusters Recalled for Undeclared Almond and Milk Allergens

    Vitamin Cottage Natural Food Markets is recalling Natural Grocers Peanut Clusters due to undeclared almond and milk allergens. Consumers should check their pantry and stop eating the product.

    Product
    NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO, 8 oz. (227g), packed in a plastic bag, UPC 000087562088, Packaged by Vitamin Cottage Natural Food Markets, Inc., Lakewood, CO 80228
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1637-2020·2020-04-08

    Bard WavelinQ 4F EndoAVF System Recalled for Magnetic Deficiency

    Bard Peripheral Vascular is recalling 150 units of the WavelinQ 4F EndoAVF System because magnetic catheters may fail to attract, potentially delaying fistula creation.

    Product
    BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, Mfr. Bard Peripheral Vascular, Inc., Ref W04200, Lot S0053, UDI (01)00801741182754(17)210215(10)S0053 - Product Usage: The WavelinQ 4F EndoAVF System in indicated for the creation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0864-2020·2020-04-08

    Meijer Mixed Nuts Recalled for Undeclared Brazil Nuts

    Meijer Inc. is recalling 8,200 packages of Mixed Nuts with Peanuts & Sea Salt due to undeclared Brazil nuts. The product was sold in six states.

    Product
    Meijer Mixed Nuts with Peanuts & Sea Salt 16 Oz UPC: 7-19283-80863-9
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1631-2020·2020-04-08

    Ra Medical Systems Recalls Pharos Excimer Laser Due to Software Error

    Ra Medical Systems is recalling 10 Pharos EX-308 Excimer Laser units because a software error may prevent the device from stopping, potentially causing skin burns.

    Product
    Pharos Excimer Laser, Model: EX-308 - Product Usage: The Pharos EX-308 Excimer Laser System is designed to treat the skin disorders psoriasis, vitiligo, atopic dermatitis, and leukoderma using phototherapy. The excimer laser system produces collimated 308 nm radiation, within…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0873-2020·2020-04-08

    Raw Seafoods Recalls Frozen Ginger Salmon for Undeclared Wheat

    Raw Seafoods Inc. is recalling 554 cases of frozen oven-safe Ginger Salmon due to undeclared wheat. The product was distributed in seven northeastern and mid-Atlantic states.

    Product
    Food You Feel Good About, Ginger Salmon, Oven Safe
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1604-2020·2020-04-08

    DeRoyal Security Cuffs Recalled for Insufficient Buckle Hold Force

    DeRoyal is recalling 94 pairs of security cuffs because the buckles do not meet required mechanical hold force standards.

    Product
    DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product Usage: patient restraint.
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·20V205000·2020-04-08

    Toyota Recalls 2020 Corolla Hatchbacks for Backup Light Failure Risk

    Toyota is recalling 2020 Corolla Hatchbacks because a damaged wire harness may cause backup lights to fail, increasing crash risk while reversing.

    Product
    TOYOTA — TOYOTA COROLLA HATCHBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V201000·2020-04-07

    Vac-Tron Recalls Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 535, MC 533 SDT, MINICOMBO, MC 573 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V204000·2020-04-07

    Vac-Tron Recalls 2012-2020 Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper exterior lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 873 SDT, MC 855 SDT, MC 833 SDT, MC 835 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V196000·2020-04-03

    Trans Tech Bus Recalls 2020 Models for Seatbelt Warning Light Defect

    Trans Tech Bus is recalling 446 specific 2020 Roadstar, SST, and ST Aero buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    TRANS TECH — TRANS TECH ROADSTAR, SST, ST AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20102·2020-04-02

    Manhattan Toy Recalls Musical Lili Llama Due to Choking Hazard

    Manhattan Toy is recalling Musical Lili Llama wooden activity toys because loose screws can fall off, posing a choking hazard to young children.

    Product
    Musical Lili Llama
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20104·2020-04-02

    VP Harrier and Giant Pinner DH Bicycle Pedals Recalled for Fall Hazards

    VP Components is recalling Harrier and Giant Pinner DH bicycle pedals because the spindle can separate from the pedal body, posing fall and injury hazards.

    Product
    VP Harrier and Giant Pinner DH bicycle pedals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20105·2020-04-02

    Stelpro Recalls Sonoma Wall Fan Heaters Due to Fire Hazard

    Stelpro Design is recalling about 3,600 Sonoma wall fan heaters because an internal part poses a fire hazard. Consumers should stop using the units and contact Stelpro for a free replacement.

    Product
    ASSO and ASSOS Sonoma wall fan heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V192000·2020-04-02

    KME Emergency Vehicles Recalled for Battery Corrosion Electrical Short Risk

    KME is recalling 2016-2020 emergency vehicles because battery corrosion can cause electrical shorts, potentially draining the battery and preventing operation during emergencies.

    Product
    KME — KME COMMERCIALCAB/ CHASSIS, PREDATOR PANTHER, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide