The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

9376–9400 of 29156

  • SevereFDA (Devices)·Z-2663-2020·2020-07-29

    Becton Dickinson Recalls PowerLoc MAX Infusion Sets Due to Tubing Cracks

    Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing may crack, risking leakage of chemicals or biohazard materials.

    Product
    PowerLoc MAX Power Injectable Infusion Set with GuardIVa Antimicrobial Hemostatic Dressing Port Access Kit; Catalog Numbers 2132010G (UDI 00801741095504), 2132015G (UDI 00801741095511), 2141910G (UDI 00801741095542), 2142010G (UDI 00801741085680), 2142015G (UDI 00801741085680), 2
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2667-2020·2020-07-29

    Becton Dickinson Recalls SafeStep Huber Needle Sets Due to Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking chemical exposure, blood loss, or infection.

    Product
    SafeStep Huber Needle Set with GuardIVa Antimicrobial Hemostatic Dressing; Catalog Number CPA00040 (UDI 00801741143892)
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2665-2020·2020-07-29

    Becton Dickinson Recalls SafeStep Huber Needle Sets Due to Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack, risking leakage of chemicals or blood.

    Product
    SafeStep Huber Needle Set myPICK Port Access Kit; Catalog Numbers CPA00020A (UDI 00801741129827), CPA00042A (UDI 00801741182969), CPA00049 (UDI 00801741175695)
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20V432000·2020-07-28

    High Altitude Trailer XT50 Recalled for Rear Swing Arm Weld Failure

    High Altitude Trailer is recalling 2019-2020 XT50 trailers with retrofitted rear swing arm spare tire carriers because a weld may fail, causing the tire to separate and increasing crash risk.

    Product
    HIGH ALTITUDE TRAILER — HIGH ALTITUDE TRAILER XT50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V434000·2020-07-28

    BMW Recalls 2019-2020 X5 and X6 M for Steering Column Defect

    BMW is recalling 2019-2020 X5 and 2020 X6 M vehicles because the steering column shaft bearing plate may not be properly attached, which can affect handling and increase crash risk.

    Product
    BMW — BMW X5, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2020·2020-07-28

    Jamaican Tastee Patties Recalls Meat and Poultry Products Lacking Federal Inspection

    Jamaican Tastee Patties, LLC is recalling approximately 60,457 pounds of beef and chicken patty products that were repackaged and relabeled without federal inspection.

    Product
    Jamaican Tastee Patties, LLC Recalls Meat and Poultry Patty Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20E051000·2020-07-28

    Meritor Recalls P220 and P579 Pressure Assemblies Due to Hose Fitting Defect

    Meritor is recalling specific pressure assemblies where an incorrect fitting may cause the power steering hydraulic hose to fail, resulting in a loss of steering assist.

    Product
    STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V435000·2020-07-28

    Daimler Recalls 2021 Thomas Built Buses Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 2021 Saf-T-Liner C2 School Buses because the brake pedal arm may rotate out of position, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V429000·2020-07-24

    Peterbilt 520 Recall: Steering Assist Bracket Bolts May Loosen

    PACCAR is recalling 2020 Peterbilt 520 trucks because incorrect bolts may allow the steering assist bracket to loosen, potentially locking the steering.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·016-2020·2020-07-24

    Coco's Italian Market Recalls Frozen Meat Products Produced Without Inspection

    Coco's Italian Market is recalling approximately 16,868 pounds of frozen meat products produced without federal inspection. No adverse reactions have been reported.

    Product
    Coco's Italian Market Recalls Italian Meatball, Beef Ravioli, and Pepperoni Pizza Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20V430000·2020-07-24

    Mercedes-Benz Recalls One 2020 GLE 350 for Seat Bolt Issue

    Mercedes-Benz is recalling one 2020 GLE 350 because a driver's seat bolt may not be installed correctly, which could increase injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20765·2020-07-23

    Polaris Recalls Ranger, PRO XD, and Bobcat Utility Vehicles Due to Crash Hazard

    Polaris is recalling approximately 13,200 Ranger, PRO XD, and Bobcat utility vehicles because a defective clutch component can cause unexpected motion, posing a crash hazard.

    Product
    Model Year 2020 Ranger XP 1000 and Ranger CREW XP 1000 Off-Road Vehicles, Model Years 2019 - 2020 PRO XD 4000D UTVs, Model Year 2019 PRO XD 2000D UTVs, and Model Year 2020 Bobcat UV34 and UV34XL UTVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2563-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Administration Sets

    CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over-infusion or under-infusion of therapy.

    Product
    BodyGuard Microset, REF: A120-161XYBS
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2587-2020·2020-07-22

    CME America Recalls CMExpress Needleless Y Site Microbore Sets

    CME America is recalling 1,824 CMExpress Needleless Y Site Microbore Sets due to delivery inaccuracy that could cause over- or under-infusion of therapy.

    Product
    CMExpress Needleless Y Site Microbore Set, REF: A120-160CYNVK
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2588-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets because they may deliver therapy at inaccurate rates, potentially causing over- or under-infusion.

    Product
    BodyGuard Microset With Female Luer, REF: A120-160XPSN
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2557-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Administration Sets

    CME America is recalling BodyGuard Microset infusion administration sets due to delivery inaccuracy that could cause over- or under-infusion of therapy.

    Product
    BodyGuard Microset, REF: A120-161XPS
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1082-2020·2020-07-22

    Fresh Express Veggie Spring Mix Recalled for Cyclospora Risk

    Fresh Express is recalling Veggie Spring Mix 7 oz. bags due to a possible health risk from Cyclospora contamination.

    Product
    Fresh Express Veggie Spring Mix 7 oz., UPC 071279281049, Baby lettuce, carrots, red cabbage & radishes
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1109-2020·2020-07-22

    Fresh Express Recalls Hy-Vee Shredded Lettuce Due to Cyclospora Risk

    Fresh Express is recalling Hy-Vee Shredded Lettuce due to a possible health risk from Cyclospora. The product was distributed in 33 U.S. states and Canada.

    Product
    Hy-Vee Shredded Lettuce 8 oz., UPC 075450120530, Iceberg lettuce
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1087-2020·2020-07-22

    Fresh Express Mediterranean Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Giant Eagle Chopped Mediterranean Salad Kits due to a possible health risk from Cyclospora.

    Product
    Giant Eagle Chopped Mediterranean Salad Kit 9.9 oz.,UPC 030034923372, Endive, cauliflower, broccoli, carrots, red cabbage & radicchio
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2573-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    BodyGuard Microset, REF: A100-163XE90S
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2569-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    CMExpress Microbore Set, REF: A120-161CYF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2564-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets due to delivery inaccuracies that may cause over- or under-infusion of therapy.

    Product
    BodyGuard Microset with Filter, REF: A100-163XESF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2583-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Sets Due to Delivery Inaccuracy

    CME America is recalling 6,320 BodyGuard Microset infusion sets because they may deliver fluids with significant inaccuracy, potentially causing over- or under-infusion of therapy.

    Product
    BodyGuard Microset with Filter and Manual Priming Valve, REF: A120-112XSFV
    Category
    Medical Device
    Distribution
    49 states