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.

16051–16075 of 29205

  • SevereFDA (Drugs)·D-0718-2017·2017-05-24

    Key Pharmacy Recalls Folinic Acid Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Folinic Acid injections because the firm cannot guarantee the products are sterile.

    Product
    FOLINIC ACID MDV (CALIF) 5MG/ML INJ, Injection, 5mg/mL, Rx only, packaged in 5 mL and10 mL glass/ Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0775-2017·2017-05-24

    FDA Recalls Compounded Progesterone Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling compounded progesterone injections because the firm cannot ensure the products are sterile.

    Product
    PROGESTERONE SESAME OIL 10ML MDV 100MG/ML INJ, Injection, 100mg/mL, Rx only, 10mL Glass; Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0786-2017·2017-05-24

    Key Pharmacy Recalls Vitamin D3 Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Vitamin D3 in Olive Oil Injection due to a lack of assurance of sterility.

    Product
    VITAMIN D3 IN OLIVE OIL SDV 100,000U/ML INJ, Injection, 150,000u/mL, Rx only, packaged in 2mL Glass/Single Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0728-2017·2017-05-24

    Key Pharmacy Recalls Hydroxo-B12 Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot guarantee the products are sterile.

    Product
    HYDROXO-B12 5ML PBF MDV (CALIF) 10MG/ML INJ, Injection, 10mg/mL, RX only, 5mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V331000·2017-05-22

    Ford Recalls 2015-2017 F-Series Trucks for Door Handle Cover Defect

    Ford is recalling specific 2015-2017 F-Series trucks equipped with chrome door handle covers that may cause doors to unlatch in a side impact, increasing injury risk.

    Product
    FORD — FORD F-150, redundant F-350, F-550, redundant F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V332000·2017-05-22

    Ford Recalls 2017 Models for Manual Seat Recliner Weld Defect

    Ford is recalling 2017 Explorer and F-Series trucks because manual seat back recliners may have inadequate welds, increasing injury risk in a crash.

    Product
    FORD — FORD EXPLORER, F-150, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V330000·2017-05-19

    Columbia Aliner Ascape Trailers Recalled for Loose Propane Gas Trays

    Columbia Northwest is recalling 2017-2018 Aliner Ascape trailers because liquid propane gas bottle trays may detach, increasing the risk of fire or crash.

    Product
    COLUMBIA — COLUMBIA ALINER ASCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·051-2017·2017-05-18

    Osso Good Co. Recalls Beef and Pork Bone Broth Products

    The Osso Good Co. is recalling approximately 1,210 pounds of beef and pork bone broth products produced without federal inspection.

    Product
    Yosemite Protein Products, Inc. — The Osso Good Co. Recalls Beef and Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·17V328000·2017-05-18

    BMW Recalls 2005-2008 7 Series Vehicles for Door Latch Defect

    BMW is recalling 2005-2008 7 Series and B7 Alpina vehicles because doors may appear latched but can unexpectedly open, risking occupant ejection.

    Product
    BMW — BMW 760LI, 750LI, 745I, 760I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2211-2017·2017-05-17

    Frito-Lay Recalls Jalapeño Flavored Potato Chips Due to Salmonella Risk

    Frito-Lay is recalling Jalapeño Flavored Lays Kettle Cooked and Miss Vickies Kettle Cooked potato chips due to a potential presence of Salmonella.

    Product
    Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape¿o Flavored Miss Vickies Kettle Cooked potato chips in the following unit sizes: 1.75 oz, 2.75 oz, 8 oz, 13.5 oz, 2.125 oz, 6.5 oz, 0.85 oz, 1.375 oz, 2.25 oz, and 1.375 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2042-2017·2017-05-17

    Arthrex Recalls Anthrex PEEK SwiveLock SP Vented Anchors Due to Breakage

    Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion. The recall covers units distributed in the US and several international locations.

    Product
    Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2045-2017·2017-05-17

    Arthrex SpeedBridge Implant System Recalled for Broken Eyelets

    Arthrex is recalling specific SpeedBridge Implant Systems because some eyelets broke during insertion. The recall covers multiple batches distributed in the US and internationally.

    Product
    Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2050-2017·2017-05-17

    Mederi Stretta Catheter Recalled Due to Sterility Compromise

    Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.

    Product
    Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. Used in the treatment of gastroesophageal reflux disease (GERD). REF 175-5580
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V324000·2017-05-17

    Isuzu Recalls NPR and GMC Trucks Due to Stuck Accelerator Pedal

    Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET, GMC NPR, W3500, W4500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2068-2017·2017-05-17

    Zimmer Biomet Recalls Regenerex Patella Implants Due to Peg Shearing

    Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.

    Product
    Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product Usage: The Regenerex Series A Patella can be used for any non-cemented resurfaced 3-peg patella application within the Vanguard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2204-2017·2017-05-17

    Del Monte Caesar Side Salad Recalled for Undeclared Allergens

    Del Monte is recalling 7-Eleven Caesar Side Salads sold in Colorado due to undeclared milk, eggs, wheat, and fish.

    Product
    7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2206-2017·2017-05-17

    Farming Fish Organic Basil Pesto Recalled for Listeria Risk

    Our Local Bounty is recalling Farming Fish brand Organic Basil Pesto with Watercress due to potential Listeria monocytogenes contamination.

    Product
    Farming Fish brand Organic Basil Pesto with Watercress, was packaged in 8.5 oz. plastic deli containers. UPC 7 23175 33586 8. The label is read in parts: "***100% Organic Basil Pesto with Watercress *** 8.5oz***Ingredients: ALL ORGANIC Basil, Watercress, Sunflower Seed Oil…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2184-2017·2017-05-17

    Rosa Foods Recalls Soylent Powder for Undeclared Milk Allergen

    Rosa Foods is recalling Soylent 1.8 Powder because it may contain undeclared milk (whey). Consumers should stop using the product.

    Product
    Soylent 1.8 Powder , 7 x 15oz pouches, SKU: 1WK-V108
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2060-2017·2017-05-17

    Savaria SL-1000 Stairlift Recalled Due to Fire Hazard

    Savaria Concord Lifts is recalling SL-1000 stairlifts because a defect in the electrical controller and motor can cause a fire.

    Product
    Savaria SL-1000 Stairlift
    Category
    Consumer Product
    Distribution
    0 states
  • SevereFDA (Food)·F-2212-2017·2017-05-17

    Frito-Lay Recalls Lays Kettle Cooked Multipacks Due to Salmonella Risk

    Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.

    Product
    12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible plastic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2205-2017·2017-05-17

    Hummingbird Wholesale Recalls Organic Cocoa-Dusted Chocolate Ginger for Undeclared Hazelnuts

    Hummingbird Wholesale is recalling Organic Cocoa-Dusted Chocolate Ginger due to undeclared hazelnuts. The product was distributed in Oregon in 5 lb. bags and bulk bins.

    Product
    Organic Cocoa-Dusted Chocolate Ginger, packaged and distributed in 5 lbs. bulk bag. Product was later offered to consumers in a self-serve bulk bin at retail store. The label is read in parts: "***Organic Cocoa-Dusted Chocolate Ginger***Made with Fair Trade 70% Dark…
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V323000·2017-05-16

    Nova Bus Recalls 2016 LFS Artic Buses for Throttle Control Defect

    Nova Bus is recalling 2016 LFS Artic transit buses because a network communication loss may cause the computer to apply full throttle without driver input.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V322000·2017-05-16

    Kenworth T800 and T880 Trucks Recalled for Brake Airline Defect

    PACCAR is recalling 2012-2018 Kenworth T800 and T880 trucks because an incorrectly sized brake control airline may increase stopping distance and crash risk.

    Product
    KENWORTH — KENWORTH T880, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17152·2017-05-15

    VanMoof Recalls B and S Series Bicycles Due to Fender Bolt Hazard

    VanMoof is recalling B and S series bicycles because front fender bolts may not break during obstructions, posing fall and impact hazards.

    Product
    VanMoof B and S series bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V311000·2017-05-11

    Toyota Recalls Tundra and Sequoia for Cracking Lugnuts

    Toyota is recalling 2013-2017 Tundra and Sequoia vehicles with specific aftermarket wheels because lugnuts may crack and detach, increasing crash risk.

    Product
    TOYOTA — TOYOTA SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide