The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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.

11401–11425 of 29162

  • SevereFDA (Devices)·Z-2446-2019·2019-09-11

    Stryker Recalls Berchtold Chromophare Monitor Carrier Arms Due to Weld Defects

    Stryker Communications is recalling 52 Berchtold Chromophare Dual Monitor Carrier Arms or Dual Flat Panels because the mounts may have insufficient welds.

    Product
    Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Food)·F-2097-2019·2019-09-11

    Mountain Mel's Peaceful Baby Herbal Tea Recalled for Salmonella Risk

    Mountain Mel's Essential Goods LLC is recalling Peaceful Baby For Colic & Teething Discomfort Herbal Tea due to potential Salmonella contamination.

    Product
    Peaceful Baby For Colic & Teething Discomfort Herbal Tea, packaged loose leaf in aluminum tin, net weight 2 oz or 56.5 grams. UPC: 7 99632 05656 0 The label is read in parts: "***Peaceful Baby FOR COLIC & TEETHING DISCOMFORT ***CAFFEINE-FREE HERBAL TEA*** Mountain Mels…
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·091-2019·2019-09-10

    Hy-Vee Recalls Ready-to-Eat Beef and Chicken for Undeclared Milk

    Hy-Vee Fresh Commissary is recalling ready-to-eat beef and chicken products because they contain undeclared milk, a known allergen.

    Product
    HY-VEE FRESH COMMISSARY — Hy-Vee Fresh Commissary Recalls Ready-To-Eat Beef and Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·19V647000·2019-09-09

    Isuzu Recalls 2017-2019 Trucks for Potential Electrical Wiring Defect

    Isuzu is recalling 2017-2019 N-Series and Chevrolet Low Cab Forward trucks because a loose bolt in the relay box may cause electrical failure and vehicle stalling.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 6500, LOW CAB FORWARD 4500, LOW CAB FORWARD 3500, N-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E060000·2019-09-06

    TAP Recalls Pro Comp Lug Nuts Due to Incorrect Sizing

    TAP Worldwide is recalling 840 Pro Comp Extended Thread lug nuts that may be incorrectly sized. The defect could prevent proper tightening, leading to lug stud failure and increased crash risk.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V643000·2019-09-06

    GM Recalls 2020 Buick Enclave and Chevrolet Traverse for Frame Rail Crack

    General Motors is recalling 2020 Buick Enclave and Chevrolet Traverse vehicles because a crack in the right-hand frame rail may reduce crash performance and increase injury risk.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V645000·2019-09-06

    GM Recalls Trucks and SUVs for Brake Vacuum Pump Defect

    General Motors is recalling 2014-2018 Chevrolet, GMC, and Cadillac vehicles because a vacuum pump defect may reduce brake assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SUBURBAN, SILVERADO 1500, SIERRA 1500, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·090-2019·2019-09-05

    BCI Foods Recalls Meat and Poultry Soup Products Lacking Import Inspection

    BCI Foods is recalling approximately 3,304 pounds of meat and poultry soup products that were imported without the required USDA inspection.

    Product
    BCI Foods Inc. Recalls Meat and Poultry Soup Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·19202·2019-09-05

    MOMO Quick Release Steering Wheel Adapters Recalled for Crash Hazard

    MW Company is recalling MOMO Quick Release Steering Wheel Adapters for race cars because the quick release mechanism can activate inadvertently, causing the steering wheel to detach and posing a crash hazard.

    Product
    MOMO Quick Release Steering Wheel Adapters for Race Cars
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2386-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc. is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393420, 14.5F, Straight, 42cm length, BARD, UDI: 00801741012228
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Devices)·Z-2378-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913230, 16F, Straight, 23cm length, BARD, UDI: 00801741013843
    Category
    Medical Device
    Distribution
    53 states
  • SevereFDA (Food)·F-2094-2019·2019-09-04

    AWERS Grained Salmon Caviar Recalled for Potential Botulism Contamination

    AWERS Inc is recalling Grained Salmon Caviar due to potential Clostridium botulinum contamination. Consumers should check their refrigerators for the specific product details.

    Product
    Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1845-2019·2019-09-04

    Pfizer Recalls Relpax Tablets Due to Microbial Contamination

    Pfizer is recalling specific lots of Relpax (eletriptan HBr) tablets because they may be contaminated with Burkholderia and Pseudomonas bacteria.

    Product
    RELPAX (eletriptan HBr) tablets, 40 mg, packaged in a) 6-count (1 card x 6 tablets) per carton, NDC 0049-2340-45; b) 12-count (2 cards x 6 tablets) per carton, NDC 0049-2340-05, Rx only, Made in Ireland, Distributed by Pfizer Roerig, Division of Pfizer Inc., NY, NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2089-2019·2019-09-04

    Confectionery Arts International Recalls Jewel Dust Pearlescent Pigment

    Confectionery Arts International is recalling Jewel Dust pearlescent pigment because borosilicate glass material was found in an FDA sample.

    Product
    All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and sold prior to 4/25/19; 4g packed in 1/4 oz. jars and 14g packed in 1 oz. jars.
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Devices)·Z-2367-2019·2019-09-04

    Siemens Artis X-Ray Systems Recalled for Patient Table Cracks

    Siemens is recalling 17 Artis zee and Artis Q interventional X-ray systems because cracks in the patient table mainframe could cause the upper bed to detach, posing a hazard to patients and staff.

    Product
    Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material Number Artis zee biplane 10094141; Artis Q floor 10848280; Artis Q biplane 10848282; Artis Q.zen floor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V640000·2019-08-30

    Lion Recalls 2018 Electric School Buses Due to Brake Connector Issue

    Lion Electric Company is recalling 2018 Lion C electric school buses because loose auxiliary brake pump connectors may cause loss of braking ability if the main pump fails.

    Product
    LION — LION LIONC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V637000·2019-08-29

    Chrysler Recalls 2019-2020 Jeep Cherokee for Steering Rack Gear Defect

    Chrysler is recalling 2019-2020 Jeep Cherokee vehicles because the steering rack gear may break, potentially causing a loss of steering control and increasing crash risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V632000·2019-08-29

    Ford Recalls 2013-2016 Fusion, MKZ, Edge, and MKX for Steering Defect

    Ford is recalling 116,160 vehicles because road salt may corrode steering bolts, causing loss of power steering assist and increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD MKZ, EDGE, FUSION, MKX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2227-2019·2019-08-28

    Edwards SAPIEN 3 Ultra Heart Valve System Recalled for Burst Balloons

    Edwards Lifesciences is recalling SAPIEN 3 Ultra Transcatheter Heart Valve Systems because burst balloons can make it difficult to remove the device from patients.

    Product
    Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Ultra Delivery System) (29mm) 9630TF29 UDI:00690103201260
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Drugs)·D-1843-2019·2019-08-28

    SCA Pharmaceuticals Recalls Ketamine Injection Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 922 syringes of Ketamine 50 mg/5 mL injection due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·19189·2019-08-28

    Whirlpool Recalls Glass Cooktops with Touch Controls Due to Burn and Fire Hazards

    Whirlpool is recalling about 26,300 glass cooktops with touch controls because the surface elements can turn on by themselves, posing burn and fire hazards.

    Product
    Whirlpool, KitchenAid and JennAir brand glass cooktops with touch controls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·087-2019·2019-08-28

    Bakkavor Recalls Chicken Salad for Undeclared Pecans and Misbranding

    Bakkavor Foods USA is recalling 1,913 pounds of ready-to-eat chicken salad products due to undeclared pecans and misbranding. The products were shipped to retail grocery locations in Texas.

    Product
    Bakkavor US - San Antonio — Bakkavor Foods USA, Inc. Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V633000·2019-08-28

    Ford Recalls 639,137 Vehicles for Defective Seat Back Recliner Mechanisms

    Ford is recalling 639,137 vehicles because a missing part in the seat back recliner mechanism may reduce strength and fail to restrain occupants in a crash.

    Product
    FORD — FORD, LINCOLN F-150, ESCAPE, F-550, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V634000·2019-08-28

    2020 MINI Cooper and JCW Recalled for Missing Rear Crash Pads

    BMW is recalling 2020 MINI Cooper, Cooper S, and JCW vehicles because rear side trim panels may lack crash pads, increasing injury risk in side impacts.

    Product
    MINI — MINI COOPER, JCW, COOPER S
    Category
    Vehicle
    Distribution
    Distributed nationwide