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.

22301–22325 of 50429

  • HighFDA (Food)·F-1295-2020·2020-09-02

    Wegmans Recalls Italian Roasted Salmon Meals Due to Listeria Risk

    Wegmans Food Markets is recalling Italian Roasted Salmon Meals because they are potentially contaminated with Listeria monocytogenes. Consumers should not eat these products.

    Product
    Italian Roasted Salmon Meals; Individual or Family Meals; plastic clamshell, package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1314-2020·2020-09-02

    Wegmans Recalls Store-Made Shrimp Salad Due to Listeria Risk

    Wegmans is recalling store-made shrimp salad sold in several states due to potential Listeria monocytogenes contamination.

    Product
    Shrimp Salad (Made In Store); by the lb.; store made shrimp salad, ready to eat; packaged in a plastic clamshell; package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·20V530000·2020-09-02

    Utilimaster Metris Recall: Incorrect Payload Labeling May Cause Tire Failure

    Shyft Group is recalling 2020 Utilimaster Metris vehicles because the payload capacity on the Tire and Loading Information label may be higher than the actual capacity, increasing the risk of tire failure and crashes.

    Product
    UTILIMASTER — UTILIMASTER METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1308-2020·2020-09-02

    Wegmans Soft Shell Crab Recalled for Listeria Contamination Risk

    Wegmans is recalling Ready to Cook Whole Soft Shell Crab with Lemon due to potential Listeria monocytogenes contamination. Consumers should check their refrigerators for this product.

    Product
    Wegmans Ready to Cook Whole Soft Shell Crab with Lemon; 11oz.; whole soft shell crab with lemon; packaged in an oven ready tray; total package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-1307-2020·2020-09-02

    Wegmans Recalls Bay Seasoned Soft Shell Crab Due to Listeria Risk

    Wegmans is recalling Bay Seasoned Soft Shell Crab potentially contaminated with Listeria monocytogenes. Consumers should discard or return the product.

    Product
    Bay Seasoned Soft Shell Crab; Individual; bay seasoned and breaded soft-shell crab; packaged in an oven ready tray; package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2840-2020·2020-09-02

    Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination

    Datascope Corporation is recalling Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall covers kits distributed worldwide.

    Product
    Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 40cc IAB Kit P/N: 0684-00-0480-01, 0684-00-0480-01U, 0684-00-0480-01C, 0684-00-0480-02, 0684-00-0480-02C, 0684-00-0480-02U, 0684-00-0480-07, 0684-00-0480-08, 0684-00-0480-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2835-2020·2020-09-02

    Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination

    Datascope is recalling 32,855 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.

    Product
    Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation 7Fr 40cc IAB Kit P/N: 0684-00-0470-01, 0684-00-0470-01U, 0684-00-0470-07, 0684-00-0470-09 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1303-2020·2020-09-02

    Wegmans Recalls Lobster Claw and Shrimp Platters Due to Listeria Risk

    Wegmans Food Markets is recalling Lobster Claw and Shrimp Platters sold in six states due to potential Listeria monocytogenes contamination.

    Product
    Lobster Claw and Shrimp Platter; Individual; lobster claw and shrimp platter with cocktail sauce and lemon wedge; packaged on a plastic tray; package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2878-2020·2020-09-02

    Ortho VITROS XT3400 Chemistry System Recalled for Erroneous Results

    Ortho Clinical Diagnostics is recalling VITROS XT3400 Chemistry Systems because slides in Slot 18 may be mis-positioned, leading to erroneous test results.

    Product
    VITROS XT3400 Chemistry System, Product code 6844458
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1315-2020·2020-09-02

    Wegmans Recalls AIP Veggie Pizzas Due to Listeria Contamination Risk

    Wegmans is recalling AIP Veggie Pizzas in several states because they may be contaminated with Listeria monocytogenes.

    Product
    AIP Veggie Pizza; Small, Medium; Large; made to order pizzas; packaged in boxes for takeout; refrigerate
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2841-2020·2020-09-02

    Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination

    Datascope Corporation is recalling 2,550 kits of Trans-Ray 7Fr 34cc Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The affected devices were distributed worldwide.

    Product
    Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB (Japan) Kit P/N: 0684-00-0545-01- Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2891-2020·2020-09-02

    Karl Storz Flexible Intubation Video Endoscope Recall for Sterilization Instructions

    Karl Storz is recalling 2,083 flexible intubation video endoscopes to provide updated sterilization instructions. The update prevents the use of specific trays and ethylene oxide sterilization to avoid introducing infectious agents into patient airways.

    Product
    Flexible Intubation Video Endoscope, Part: 11301BNX, with Instruction Manual: Z18444US - Product Usage: are intended to be used for examination and visualization of a patient s upper airway and for aiding placement of an endotracheal tube.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2855-2020·2020-09-02

    Globus Medical Recalls Specific Lots of ALTERA Spacers Due to Material Error

    Globus Medical is recalling specific lots of ALTERA Spacers because internal components may have been manufactured using stainless steel instead of the specified cobalt chromium molybdenum alloy.

    Product
    ALTERA Spacer ALTERA Spacer, 10x26, 9-13mm, 15¿
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1293-2020·2020-09-02

    Wegmans Recalls Chicken Cutlets Due to Listeria Contamination Risk

    Wegmans Food Markets is recalling specific chicken cutlets sold in the Northeast and Mid-Atlantic regions due to potential Listeria monocytogenes contamination.

    Product
    Wegmans Chicken Cutlet; by the lb, in a meal or in a 22 oz. Family Pack; "Heating Instructions: Oven-Preheat to 400 degrees F. Remove chicken from package and place on baking sheet pan. Bake 5-7 minutes. Microwave-Remove label/lid. Heat 2-3 minutes"; Keep Refrigerated; packaged…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2881-2020·2020-09-02

    Klarity Vacuum Bags Recalled for Inadequate Vacuum Retention During Radiation Therapy

    Klarity Medical Products LLC is recalling 111 vacuum bags used for patient positioning during radiation therapy because they may not hold a vacuum adequately for the required treatment time.

    Product
    Klarity Vacuum Bags, Item Nos. R7504-30C, R7504-35BC,R7504-35C, R7644-32.5BC, RC7221-25BC, RC7504-17.5C - Product Usage: To be used by trained medical professionals for the stable support and positioning of patients undergoing external beam radiation therapy treatment in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1311-2020·2020-09-02

    Wegmans Recalls Seasoned Whole Rainbow Trout Due to Listeria Risk

    Wegmans Food Markets is recalling seasoned whole rainbow trout potentially contaminated with Listeria monocytogenes. Consumers should check their refrigerators and discard or return the product.

    Product
    Seasoned Whole Rainbow Trout; by the lb.; seasoned rainbow trout; packaged in an oven ready tray; package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2820-2020·2020-09-02

    89 North LDI Laser Firmware Recall for Safety Interlock Defect

    89 North is recalling 188 LDI laser units worldwide due to a firmware defect that allows laser emission to continue when safety interlocks are opened.

    Product
    LDI Laser firmware lower than V02.13.00 for LDI models: LDl-7, LDI-WF, LDI-NIR, LDl-6 Laser Science fluorescence imaging
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2906-2020·2020-09-02

    Neurovision Cobra x5 EMG Endotracheal Tubes Recalled for Insulation Defect

    Neurovision is recalling Cobra x5 EMG endotracheal tubes because the electrode insulation may soften and damage, potentially stopping EMG signal transmission.

    Product
    Cobra x5 2-Ch EMG ET Tube, 6.0mm, REF: LTE700DCS-5, Rx Only, Sterile EO UDI: B006LTE700DCS52/$$7062618C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2863-2020·2020-09-02

    Globus Medical Recalls Specific Lots of ALTERA Spacers Due to Material Error

    Globus Medical is recalling specific lots of ALTERA Spacers because internal components may have been manufactured using stainless steel instead of the specified cobalt chromium molybdenum alloy.

    Product
    ALTERA Spacer ALTERA Spacer, 10x31, 10-14mm, 15¿
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2907-2020·2020-09-02

    Neurovision Cobra x5 EMG ET Tube Recalled for Insulation Softening

    Neurovision is recalling Cobra x5 2-Ch EMG ET Tubes because the electrode insulating material may soften over time, potentially damaging the device and stopping EMG signal transmission.

    Product
    Cobra x5 2-Ch EMG ET Tube, 7.0mm, REF: LTE700DCM-5, Rx Only, Sterile EO UDI: B006LTE700DCM52 - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1302-2020·2020-09-02

    Wegmans Recalls Fresh Cooked Shrimp and Crab Claw Tray for Listeria Risk

    Wegmans Food Markets is recalling fresh cooked shrimp and crab claw trays due to potential Listeria monocytogenes contamination. Consumers should not eat the product.

    Product
    Fresh Cooked Shrimp and Crab Claw Tray; Individual; shrimp and crab claw platter with cocktail sauce; packaged in a plastic tray; package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2845-2020·2020-09-02

    Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination

    Datascope Corporation is recalling 6,111 Intra-Aortic Balloon Catheter kits due to potential endotoxin contamination. The affected products were distributed worldwide.

    Product
    Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB (Japan) Kit P/N: 0684-00-0559-01 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1312-2020·2020-09-02

    Wegmans Recalls Whole Seasoned Snapper Due to Listeria Contamination Risk

    Wegmans is recalling Whole Seasoned Snapper sold in several states because it may be contaminated with Listeria monocytogenes.

    Product
    Whole Seasoned Snapper; by the lb.; whole seasoned snapper with lemon and oil; packaged in an oven ready tray; total package size varies; keep refrigerated
    Category
    Food
    Distribution
    6 states